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                "name": "Rab protein signal transduction",
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        "protein_name": "Anaphase-promoting complex subunit 5",
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                "name": "cytoplasm",
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                "name": "cell division",
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                "pmid": ""
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                "name": "regulation of proteolysis",
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                ],
                "pmid": ""
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            {
                "name": "protein ubiquitination",
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            {
                "name": "anaphase-promoting complex-dependent catabolic process",
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                    {
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                ],
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            },
            {
                "name": "protein K11-linked ubiquitination",
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                    {
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                "name": "axonemal dynein complex assembly",
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                "name": "Golgi cisterna membrane",
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                "description": "A lacrimal apparatus disease that is characterized by persistent irritation or burning of the coreneal surface.",
                "url": "https://disease-ontology.org/term/DOID:10140",
                "evidence": [
                    {
                        "id": "10140",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10140"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11054",
                "name": "urinary bladder cancer",
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder.",
                "url": "https://disease-ontology.org/term/DOID:11054",
                "evidence": [
                    {
                        "id": "11054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11054"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11204",
                "name": "allergic conjunctivitis",
                "description": "A chronic conjunctivitis that is an inflammation of the conjunctiva involing red, itchy, and watery eyes a resulting from an exposure to an allergen or an irritant.",
                "url": "https://disease-ontology.org/term/DOID:11204",
                "evidence": [
                    {
                        "id": "11204",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11204"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11339",
                "name": "pneumocystosis",
                "description": "An opportunistic mycosis that is located in lungs, but can also occur in eyes, ears, skin, thyroid, pituitary, palate, parathyroid, esophagus, pleura, heart, liver, spleen, small intestine, adrenals, kidneys, bone marrow, and lymph nodes, has_material_basis_in Pneumocystis jirovecii that effects interstitial and alveolar tissues and has symptom nonproductive cough, has symptom shortness of breath, and has symptom fever.",
                "url": "https://disease-ontology.org/term/DOID:11339",
                "evidence": [
                    {
                        "id": "11339",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11339"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11394",
                "name": "adult respiratory distress syndrome",
                "description": "A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia.",
                "url": "https://disease-ontology.org/term/DOID:11394",
                "evidence": [
                    {
                        "id": "11394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:114",
                "name": "heart disease",
                "description": "A cardiovascular system disease that involves the heart.",
                "url": "https://disease-ontology.org/term/DOID:114",
                "evidence": [
                    {
                        "id": "114",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:114"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11650",
                "name": "bronchopulmonary dysplasia",
                "description": "A lung disease that is characterized by underdeveloped lungs in newborns that can be easily irritated or inflamed after birth resulting in damage to the alveoli of the lungs and bronchi. Most newborns who develop BPD are born more than 10 weeks before their due dates, weigh less than 2 pounds at birth, and have breathing problems.",
                "url": "https://disease-ontology.org/term/DOID:11650",
                "evidence": [
                    {
                        "id": "11650",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11650"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13406",
                "name": "pulmonary sarcoidosis",
                "description": "A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction.",
                "url": "https://disease-ontology.org/term/DOID:13406",
                "evidence": [
                    {
                        "id": "13406",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13406"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13891",
                "name": "bird fancier's lung",
                "description": "An extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta. The disease has_symptom abrupt onset of dyspnea, has_symptom cough, has_symptom malaise, and has_symptom fever, after exposure to antigen.",
                "url": "https://disease-ontology.org/term/DOID:13891",
                "evidence": [
                    {
                        "id": "13891",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13891"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2799",
                "name": "bronchiolitis obliterans",
                "description": "A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults.",
                "url": "https://disease-ontology.org/term/DOID:2799",
                "evidence": [
                    {
                        "id": "2799",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2799"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3030",
                "name": "mucinous adenocarcinoma",
                "description": "An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin.",
                "url": "https://disease-ontology.org/term/DOID:3030",
                "evidence": [
                    {
                        "id": "3030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3082",
                "name": "interstitial lung disease",
                "description": "A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough.",
                "url": "https://disease-ontology.org/term/DOID:3082",
                "evidence": [
                    {
                        "id": "3082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3458",
                "name": "breast adenocarcinoma",
                "description": "A breast carcinoma that originates in the milk ducts and/or lobules (glandular tissue) of the breast.",
                "url": "https://disease-ontology.org/term/DOID:3458",
                "evidence": [
                    {
                        "id": "3458",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3458"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4481",
                "name": "allergic rhinitis",
                "description": "A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites.",
                "url": "https://disease-ontology.org/term/DOID:4481",
                "evidence": [
                    {
                        "id": "4481",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4481"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4608",
                "name": "common bile duct neoplasm",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4608",
                "evidence": [
                    {
                        "id": "4608",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4608"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4947",
                "name": "cholangiocarcinoma",
                "description": "A bile duct adenocarcinoma that has_material_basis_in bile duct epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:4947",
                "evidence": [
                    {
                        "id": "4947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:552",
                "name": "pneumonia",
                "description": "A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing.",
                "url": "https://disease-ontology.org/term/DOID:552",
                "evidence": [
                    {
                        "id": "552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:850",
                "name": "lung disease",
                "description": "A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide.",
                "url": "https://disease-ontology.org/term/DOID:850",
                "evidence": [
                    {
                        "id": "850",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:850"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8622",
                "name": "measles",
                "description": "A viral infectious disease that results_in infection located_in skin, has_material_basis_in Measles virus (Morbillivirus hominis), which is transmitted_by contact with oronasal secretions, or semen of an infected person. The infection has_symptom fever, has_symptom cough, has_symptom coryza, has_symptom conjunctivitis, and has_symptom maculopapular, erythematous rash.",
                "url": "https://disease-ontology.org/term/DOID:8622",
                "evidence": [
                    {
                        "id": "8622",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8622"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "extracellular matrix structural constituent",
                "id": "GO:0005201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBD0",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBD0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "X2JBD0-1",
                "start_pos": "292",
                "end_pos": "292",
                "site_lbl": "Thr292",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 292,
                        "start_aa": "Thr",
                        "end_pos": 292,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr292",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "X2JBD0-1",
                "start_pos": "86",
                "end_pos": "86",
                "site_lbl": "Thr86",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 86,
                        "start_aa": "Thr",
                        "end_pos": 86,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr86",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "X2JBL3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JBL3",
                        "url": "https://www.uniprot.org/uniprotkb/X2JBL3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 187,
        "chemical_mass": 20848.0,
        "gene_names": "Dmel\\CG44437;CG1903;CG44437;Dmel\\CG44437;Dmel_CG44437",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "X2JCU8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 964,
        "chemical_mass": 104576.0,
        "gene_names": "CG14126;CG5917;CG14126;CG14129;CG34420;CG44837;CG5917;Dmel\\CG44837;Dmel_CG44837",
        "protein_name": "Dipeptidase",
        "disease": [],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metallodipeptidase activity",
                "id": "GO:0070573",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070573",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dipeptidase activity",
                "id": "GO:0016805",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016805",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "side of membrane",
                "id": "GO:0098552",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098552",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCU8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCU8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
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                "name": "Golgi membrane",
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                "name": "COPII-coated ER to Golgi transport vesicle",
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                "pmid": ""
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                "pmid": ""
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                "name": "endoplasmic reticulum exit site",
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                "pmid": ""
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                "name": "Golgi stack",
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                "pmid": ""
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                "pmid": ""
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                "name": "zinc ion binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                ],
                "pmid": ""
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                ],
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            },
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                ],
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            },
            {
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                "name": "sensory perception of touch",
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            {
                "name": "detection of mechanical stimulus involved in sensory perception of pain",
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                "pmid": ""
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            {
                "name": "sodium ion transmembrane transport",
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            {
                "name": "sodium ion transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
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                "pmid": ""
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        ],
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                "name": "plasma membrane",
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                ],
                "pmid": ""
            },
            {
                "name": "membrane",
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                "pmid": ""
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            {
                "name": "axon",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424",
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                ],
                "pmid": ""
            },
            {
                "name": "dendrite",
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                ],
                "pmid": ""
            },
            {
                "name": "neuronal cell body",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4K691"
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                ],
                "pmid": ""
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        ],
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            {
                "name": "sodium channel activity",
                "id": "GO:0005272",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005272",
                "evidence": [
                    {
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                ],
                "pmid": ""
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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                        "site_category_dict": {
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                ]
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                ],
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        ],
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            {
                "name": "basal cortex",
                "id": "GO:0045180",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045180",
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                "pmid": ""
            },
            {
                "name": "lamellipodium",
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                ],
                "pmid": ""
            },
            {
                "name": "basal part of cell",
                "id": "GO:0045178",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045178",
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                ],
                "pmid": ""
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            {
                "name": "perinuclear region of cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
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                        "database": "UniProtKB",
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                "pmid": ""
            },
            {
                "name": "SCAR complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031209",
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            {
                "name": "lamellipodium membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031258",
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                "pmid": ""
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            {
                "name": "protein-containing complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032991",
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                "pmid": ""
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                "name": "actin-based cell projection",
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        ],
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                "name": "positive regulation of cytoskeleton organization",
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                "name": "establishment of planar polarity of follicular epithelium",
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            {
                "name": "cell adhesion",
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                "name": "neuromuscular junction development",
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                        "database": "UniProtKB",
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            {
                "name": "regulation of actin cytoskeleton organization",
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            {
                "name": "neuron migration",
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                "pmid": ""
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            {
                "name": "actin cytoskeleton organization",
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            {
                "name": "cell adhesion mediated by integrin",
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            {
                "name": "positive regulation of stress fiber assembly",
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            {
                "name": "regulation of cell shape",
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                "name": "cortical actin cytoskeleton organization",
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    },
    {
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            {
                "name": "plasma membrane",
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                "name": "plasma membrane phospholipid scrambling",
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                "name": "phospholipid scramblase activity",
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                ],
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        ],
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                    {
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                "pmid": ""
            },
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                "name": "nuclear localization sequence binding",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nuclear pore cytoplasmic filaments",
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                    {
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                ],
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            }
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "telomere tethering at nuclear periphery",
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                ],
                "pmid": ""
            },
            {
                "name": "RNA export from nucleus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006405",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KEV6"
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                ],
                "pmid": ""
            },
            {
                "name": "protein import into nucleus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006606",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KEV6",
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                    }
                ],
                "pmid": ""
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        ],
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                ],
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            {
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                    }
                ],
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            },
            {
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                "evidence": [
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                ],
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                "name": "aminoacyl-tRNA deacylase activity",
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                ],
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                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KF06"
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                ],
                "pmid": ""
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        ],
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                "name": "valyl-tRNA aminoacylation",
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        ],
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                "name": "cytoplasm",
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                ],
                "pmid": ""
            },
            {
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                ],
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        ],
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                ],
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                ],
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            },
            {
                "name": "chromatin organization",
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                ],
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            {
                "name": "hindgut morphogenesis",
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                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
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                ],
                "pmid": ""
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            {
                "name": "regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
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                ],
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            },
            {
                "name": "cell migration",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016477",
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                        "id": "A0A0B4KFC4",
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                "pmid": ""
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            {
                "name": "regulation of DNA-templated transcription",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
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                ],
                "pmid": ""
            },
            {
                "name": "membrane organization",
                "id": "GO:0061024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061024",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "central nervous system development",
                "id": "GO:0007417",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007417",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoskeleton organization",
                "id": "GO:0007010",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007010",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell shape",
                "id": "GO:0008360",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008360",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular protein localization",
                "id": "GO:0008104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008104",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "salivary gland development",
                "id": "GO:0007431",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007431",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "salivary gland morphogenesis",
                "id": "GO:0007435",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007435",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "gonad development",
                "id": "GO:0008406",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008406",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "establishment or maintenance of epithelial cell apical/basal polarity",
                "id": "GO:0045197",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045197",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal closure",
                "id": "GO:0007391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "open tracheal system development",
                "id": "GO:0007424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tracheal outgrowth, open tracheal system",
                "id": "GO:0007426",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007426",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial cell migration, open tracheal system",
                "id": "GO:0007427",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007427",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Malpighian tubule morphogenesis",
                "id": "GO:0007443",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007443",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "head involution",
                "id": "GO:0008258",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008258",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of Malpighian tubule diameter",
                "id": "GO:0035297",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035297",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity",
                "id": "GO:0003700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFC4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFC4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A0B4KFC4-1",
                "start_pos": "141",
                "end_pos": "141",
                "site_lbl": "Thr141",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 141,
                        "start_aa": "Thr",
                        "end_pos": 141,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr141",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A0B4KFC4-1",
                "start_pos": "5",
                "end_pos": "5",
                "site_lbl": "Thr5",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 5,
                        "start_aa": "Thr",
                        "end_pos": 5,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr5",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KFK6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 582,
        "chemical_mass": 64311.0,
        "gene_names": "Dmel\\CG4630;CG4630;Dmel\\CG4630;Dmel_CG4630",
        "protein_name": "Major facilitator superfamily (MFS) profile domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:0050700",
                "evidence": [
                    {
                        "id": "0050700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050908",
                "name": "myelodysplastic syndrome",
                "description": "A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets.",
                "url": "https://disease-ontology.org/term/DOID:0050908",
                "evidence": [
                    {
                        "id": "0050908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14365",
                "name": "systemic primary carnitine deficiency disease",
                "description": "An amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy.",
                "url": "https://disease-ontology.org/term/DOID:14365",
                "evidence": [
                    {
                        "id": "14365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:655",
                "name": "inherited metabolic disorder",
                "description": "A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.",
                "url": "https://disease-ontology.org/term/DOID:655",
                "evidence": [
                    {
                        "id": "655",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:655"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7148",
                "name": "rheumatoid arthritis",
                "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:7148",
                "evidence": [
                    {
                        "id": "7148",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7148"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
                "description": "An intestinal disease that involves inflammation located_in intestine.",
                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFK6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFK6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KFW6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KFW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KFW6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 154,
        "chemical_mass": 17817.0,
        "gene_names": "Dmel\\CG43709;CG43709;Dmel\\CG43709;Dmel_CG43709",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KG18-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG18",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG18"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 72,
        "chemical_mass": 8526.0,
        "gene_names": "Dmel\\CG43829;CG43829;Dmel\\CG43829;Dmel_CG43829",
        "protein_name": "Seminal fluid protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KG96-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 827,
        "chemical_mass": 92360.0,
        "gene_names": "hrg;CG9854;Dmel\\CG9854;Dmel_CG9854;Hiiragi;PAP;Pap;dHrg;hrg;l(2)07619;l(2)k07619",
        "protein_name": "polynucleotide adenylyltransferase",
        "disease": [],
        "molecular_function": [
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "poly(A) RNA polymerase activity",
                "id": "GO:1990817",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990817",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cytosolic mRNA polyadenylation",
                "id": "GO:0180011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0180011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "co-transcriptional mRNA 3'-end processing, cleavage and polyadenylation pathway",
                "id": "GO:0180010",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0180010",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KG96",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KG96"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A0B4KG96-1",
                "start_pos": "824",
                "end_pos": "824",
                "site_lbl": "Thr824",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 824,
                        "start_aa": "Thr",
                        "end_pos": 824,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr824",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4KGS4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KGS4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KGS4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 583,
        "chemical_mass": 65784.0,
        "gene_names": "Pak3;CG14895;D-Pak3;DPAK3;DPak3;DmPAK3;Dmel\\CG14895;Dmel_CG14895;Dpak3;PAK-3;PAK3;PaK3;Pak3;Pak;anon-WO0118547.285;dPAK3;dpak3;pak3",
        "protein_name": "non-specific serine/threonine protein kinase",
        "disease": [],
        "biological_process": [
            {
                "name": "regulation of axonogenesis",
                "id": "GO:0050770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050770",
                "evidence": [
                    {
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                "name": "actin filament organization",
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                "pmid": ""
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                "pmid": ""
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            {
                "name": "intracellular signal transduction",
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                "name": "myoblast fusion",
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                "name": "cellular response to starvation",
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                "pmid": ""
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                "name": "cell projection organization",
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                "name": "regulation of MAPK cascade",
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                "name": "border follicle cell migration",
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                "pmid": ""
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                "name": "protein serine/threonine kinase activity",
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                    {
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                "pmid": ""
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                "pmid": ""
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            {
                "name": "small GTPase binding",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
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                ],
                "pmid": ""
            },
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                "name": "ruffle",
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                    {
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                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    {
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            {
                "name": "Drosophila melanogaster",
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        "molecular_function": [
            {
                "name": "ecdysteroid 22-kinase activity",
                "id": "GO:0106389",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
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    {
        "uniprot_canonical_ac": "A0A0B4KH11-1",
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                    {
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        "protein_name": "",
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    },
    {
        "uniprot_canonical_ac": "A0A0B4KH75-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "A0A0B4KH75",
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                ],
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        "gene_names": "BcDNA:RE40372;BcDNA:RE40372;CG31446;Dmel\\CG31446;Dmel_CG31446",
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    },
    {
        "uniprot_canonical_ac": "A0A0B4KHM5-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
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        "protein_name": "Major facilitator superfamily (MFS) profile domain-containing protein",
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        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KHM5",
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                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KHM5"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KHM5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KHM5"
                    }
                ],
                "pmid": ""
            }
        ],
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    {
        "uniprot_canonical_ac": "A0A0B4KI55-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "A0A0B4KI55",
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                ],
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        ],
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        "protein_name": "Dynein assembly factor with WDR repeat domains 1",
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                "disease_id": "DOID:0050144",
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                "url": "https://disease-ontology.org/term/DOID:0050144",
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                    {
                        "id": "0050144",
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                ],
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            },
            {
                "disease_id": "DOID:0050545",
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                "url": "https://disease-ontology.org/term/DOID:0050545",
                "evidence": [
                    {
                        "id": "0050545",
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                ],
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            },
            {
                "disease_id": "DOID:9562",
                "name": "primary ciliary dyskinesia",
                "description": "A ciliopathy that is characterized by impaired function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) and fallopian tube.",
                "url": "https://disease-ontology.org/term/DOID:9562",
                "evidence": [
                    {
                        "id": "9562",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9562"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "SCF ubiquitin ligase complex",
                "id": "GO:0019005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KI55",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KI55"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein polyubiquitination",
                "id": "GO:0000209",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000209",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KI55",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KI55"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonemal dynein complex assembly",
                "id": "GO:0070286",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070286",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KI55",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KI55"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ubiquitin-like ligase-substrate adaptor activity",
                "id": "GO:1990756",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990756",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4KI55",
                        "url": "https://www.uniprot.org/uniprotkb/A0A0B4KI55"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A0A0B4LED6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A0B4LED6",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 6290.0,
        "gene_names": "lincRNA.249;CG44438;Dmel\\CG44438;Dmel_CG44438;lincRNA.249",
        "protein_name": "",
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        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A1Z7M8-1",
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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        "chemical_mass": 70158.0,
        "gene_names": "Ance-4;Ance-4;CG8196;Dmel\\CG8196;Dmel_CG8196;ance-4",
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                "disease_id": "DOID:0050152",
                "name": "aspiration pneumonia",
                "description": "A bacterial pneumonia which is an acute pulmonary inflammatory response that develops after the inhalation of colonized oropharyngeal material containing bacteria. It is seen in individuals with dysphagia and gastric dysmotility. The disease has_symptom tachypnea and has_symptom cough.",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050152"
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                ],
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            {
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                "evidence": [
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                        "id": "0050848",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050848"
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                ],
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            },
            {
                "disease_id": "DOID:0050855",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050855"
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                "url": "https://disease-ontology.org/term/DOID:0051061",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
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                "url": "https://disease-ontology.org/term/DOID:0060224",
                "evidence": [
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                        "id": "0060224",
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            },
            {
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                "evidence": [
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                        "url": "https://www.alliancegenome.org/disease/DOID:0070658"
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                ],
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            },
            {
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                "evidence": [
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080599"
                    }
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            },
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                "url": "https://disease-ontology.org/term/DOID:0080600",
                "evidence": [
                    {
                        "id": "0080600",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080600"
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                "weight": 0.0
            },
            {
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                "description": "A gastrointestinal system cancer that is located_in the stomach.",
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                "evidence": [
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                        "id": "10534",
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                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
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            },
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                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10952",
                "name": "nephritis",
                "description": "A kidney disease that is characterized by an inflammation of the kidneys.",
                "url": "https://disease-ontology.org/term/DOID:10952",
                "evidence": [
                    {
                        "id": "10952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10952"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11123",
                "name": "IgA vasculitis",
                "description": "A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.",
                "url": "https://disease-ontology.org/term/DOID:11123",
                "evidence": [
                    {
                        "id": "11123",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11123"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11335",
                "name": "sarcoidosis",
                "description": "A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs.",
                "url": "https://disease-ontology.org/term/DOID:11335",
                "evidence": [
                    {
                        "id": "11335",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11335"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11400",
                "name": "pyelonephritis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11400",
                "evidence": [
                    {
                        "id": "11400",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11400"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11713",
                "name": "diabetic angiopathy",
                "description": "A peripheral vascular disease that is characterized by narrowing of the arteries as a complication arising from chronic diabetes.",
                "url": "https://disease-ontology.org/term/DOID:11713",
                "evidence": [
                    {
                        "id": "11713",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11713"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1205",
                "name": "allergic disease",
                "description": "An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.",
                "url": "https://disease-ontology.org/term/DOID:1205",
                "evidence": [
                    {
                        "id": "1205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1240",
                "name": "leukemia",
                "description": "A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells.",
                "url": "https://disease-ontology.org/term/DOID:1240",
                "evidence": [
                    {
                        "id": "1240",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1240"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12549",
                "name": "hepatitis A",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis A virus (Hepatovirus ahepa), which is transmitted_by ingestion of contaminated food or water, or transmitted_by direct contact with an infected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice.",
                "url": "https://disease-ontology.org/term/DOID:12549",
                "evidence": [
                    {
                        "id": "12549",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12549"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
                "description": "An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes.",
                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14499",
                "name": "Fabry disease",
                "description": "A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.",
                "url": "https://disease-ontology.org/term/DOID:14499",
                "evidence": [
                    {
                        "id": "14499",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14499"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2987",
                "name": "familial Mediterranean fever",
                "description": "An autoinflammatory disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin.",
                "url": "https://disease-ontology.org/term/DOID:2987",
                "evidence": [
                    {
                        "id": "2987",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2987"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3500",
                "name": "gallbladder adenocarcinoma",
                "description": "A gallbladder carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3500",
                "evidence": [
                    {
                        "id": "3500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3500"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain.",
                "url": "https://disease-ontology.org/term/DOID:3526",
                "evidence": [
                    {
                        "id": "3526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3905",
                "name": "lung carcinoma",
                "description": "A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis.",
                "url": "https://disease-ontology.org/term/DOID:3905",
                "evidence": [
                    {
                        "id": "3905",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3905"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4079",
                "name": "heart valve disease",
                "description": "A heart disease involving one or more of the four valves of the heart (the aortic and mitral valves on the left and the pulmonary and tricuspid valves on the right).",
                "url": "https://disease-ontology.org/term/DOID:4079",
                "evidence": [
                    {
                        "id": "4079",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4079"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:552",
                "name": "pneumonia",
                "description": "A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing.",
                "url": "https://disease-ontology.org/term/DOID:552",
                "evidence": [
                    {
                        "id": "552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:576",
                "name": "proteinuria",
                "description": "A kidney disease that is characterized by the presence of excess proteins in the urine.",
                "url": "https://disease-ontology.org/term/DOID:576",
                "evidence": [
                    {
                        "id": "576",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:576"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:61",
                "name": "mitral valve disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:61",
                "evidence": [
                    {
                        "id": "61",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:61"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7147",
                "name": "ankylosing spondylitis",
                "description": "An arthritis that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage.",
                "url": "https://disease-ontology.org/term/DOID:7147",
                "evidence": [
                    {
                        "id": "7147",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7147"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:841",
                "name": "extrinsic allergic alveolitis",
                "description": "An interstitial lung disease involving inflammation of alveoli and smallest airways (bronchioles) of the lung caused by an allergic reaction to inhaled organic dusts containing microorganisms or proteins, and chemicals. Symptoms include chills, cough, fever, malaise, shortness of breath, loss of appetite and weight loss.",
                "url": "https://disease-ontology.org/term/DOID:841",
                "evidence": [
                    {
                        "id": "841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8432",
                "name": "polycythemia",
                "description": "A bone marrow disease characterized by an increased number of red blood cells in the bloodstream resulting in thicker blood and reduced blood flow.",
                "url": "https://disease-ontology.org/term/DOID:8432",
                "evidence": [
                    {
                        "id": "8432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8552",
                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
                "evidence": [
                    {
                        "id": "8552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8805",
                "name": "intermediate coronary syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8805",
                "evidence": [
                    {
                        "id": "8805",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8805"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8970",
                "name": "subacute sclerosing panencephalitis",
                "description": "A viral encephalitis that has_material_basis_in persistent central nervous system infection of the wild-type measles virus (Morbillivirus hominis) characterized by onset of personality or behavioral changes and intellectual deterioriation years after initial infection, followed by progressive decline in motor function, akinetic mutism or coma, and death. Higher incidence or shorter latency periods may be observed in those initially infected under the age of 2 or in cases of intrafamilial transmission.",
                "url": "https://disease-ontology.org/term/DOID:8970",
                "evidence": [
                    {
                        "id": "8970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8970"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9538",
                "name": "multiple myeloma",
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow.",
                "url": "https://disease-ontology.org/term/DOID:9538",
                "evidence": [
                    {
                        "id": "9538",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9538"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9775",
                "name": "diastolic heart failure",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9775",
                "evidence": [
                    {
                        "id": "9775",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9775"
                    }
                ],
                "weight": 0.0
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                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13207",
                "name": "proliferative diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13207",
                "evidence": [
                    {
                        "id": "13207",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13207"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13514",
                "name": "venous tributary occlusion of retina",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13514",
                "evidence": [
                    {
                        "id": "13514",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13514"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
                    {
                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1727",
                "name": "retinal vein occlusion",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1727",
                "evidence": [
                    {
                        "id": "1727",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1727"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2154",
                "name": "nephroblastoma",
                "description": "A kidney cancer that affects the kidneys and typically occuring in children.",
                "url": "https://disease-ontology.org/term/DOID:2154",
                "evidence": [
                    {
                        "id": "2154",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2154"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:289",
                "name": "endometriosis",
                "description": "A female reproductive system disease characterized by the growth of endometrial tissue outside the uterine body.",
                "url": "https://disease-ontology.org/term/DOID:289",
                "evidence": [
                    {
                        "id": "289",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:289"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.",
                "url": "https://disease-ontology.org/term/DOID:332",
                "evidence": [
                    {
                        "id": "332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3347",
                "name": "osteosarcoma",
                "description": "A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus).",
                "url": "https://disease-ontology.org/term/DOID:3347",
                "evidence": [
                    {
                        "id": "3347",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3347"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4448",
                "name": "macular degeneration",
                "description": "A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.",
                "url": "https://disease-ontology.org/term/DOID:4448",
                "evidence": [
                    {
                        "id": "4448",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4448"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4449",
                "name": "macular retinal edema",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4449",
                "evidence": [
                    {
                        "id": "4449",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4449"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4724",
                "name": "brain edema",
                "description": "A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.",
                "url": "https://disease-ontology.org/term/DOID:4724",
                "evidence": [
                    {
                        "id": "4724",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4724"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5052",
                "name": "melioidosis",
                "description": "A primary bacterial infectious disease that results_in infection, has_material_basis_in Burkholderia pseudomallei, which is transmitted_by contact with the contaminated water or soil. The infection has_symptom fever, has_symptom respiratory distress, has_symptom chest pain, and has_symptom stomach pain.",
                "url": "https://disease-ontology.org/term/DOID:5052",
                "evidence": [
                    {
                        "id": "5052",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5052"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5425",
                "name": "ovarian hyperstimulation syndrome",
                "description": "An ovarian disease that is characterized by cystic enlargement of the ovaries and a fluid shift from the intravascular to the third space and has_symptom abdominal pain, has_symptom nausea and has_symptom vomiting. This disease is an iatrogenic complication of assisted reproduction technology.",
                "url": "https://disease-ontology.org/term/DOID:5425",
                "evidence": [
                    {
                        "id": "5425",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5425"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:768",
                "name": "retinoblastoma",
                "description": "A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina.",
                "url": "https://disease-ontology.org/term/DOID:768",
                "evidence": [
                    {
                        "id": "768",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:768"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7998",
                "name": "hyperthyroidism",
                "description": "A thyroid gland disease that involves an over production of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:7998",
                "evidence": [
                    {
                        "id": "7998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8466",
                "name": "retinal degeneration",
                "description": "A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina.",
                "url": "https://disease-ontology.org/term/DOID:8466",
                "evidence": [
                    {
                        "id": "8466",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8466"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8544",
                "name": "chronic fatigue syndrome",
                "description": "A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions.",
                "url": "https://disease-ontology.org/term/DOID:8544",
                "evidence": [
                    {
                        "id": "8544",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8544"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9719",
                "name": "neovascular inflammatory vitreoretinopathy",
                "description": "A retinal and vitreous disease characterized by ocular inflammation, vascular dropout, large spots of hyperpigmentation, neovascularization of the peripheral and posterior retina, vitreous hemorrhage, and retinal detachment that has_material_basis_in heterozygous mutation in the CAPN5 gene on chromosome 11q13.5.",
                "url": "https://disease-ontology.org/term/DOID:9719",
                "evidence": [
                    {
                        "id": "9719",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9719"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6I3",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6I3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "peptidase inhibitor activity",
                "id": "GO:0030414",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030414",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6I3",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6I3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of immune response",
                "id": "GO:0050776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050776",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6I3",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6I3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A1Z6I3-1",
                "start_pos": "20",
                "end_pos": "20",
                "site_lbl": "Thr20",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 20,
                        "start_aa": "Thr",
                        "end_pos": 20,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr20",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A1Z6I3-1",
                "start_pos": "313",
                "end_pos": "313",
                "site_lbl": "Thr313",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 313,
                        "start_aa": "Thr",
                        "end_pos": 313,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr313",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A1Z6J2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1276,
        "chemical_mass": 142495.0,
        "gene_names": "SCAP;CG14592;CG33131;CG8356;Dmel\\CG33131;Dmel_CG33131;SCAP;Scap_Dm;Scap;dSCAP;dScap;dscap",
        "protein_name": "Sterol regulatory element-binding protein cleavage-activating protein",
        "disease": [
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ER to Golgi transport vesicle membrane",
                "id": "GO:0012507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SREBP-SCAP complex",
                "id": "GO:0032936",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032936",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "fatty acid metabolic process",
                "id": "GO:0006631",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006631",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cholesterol metabolic process",
                "id": "GO:0008203",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008203",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cholesterol biosynthetic process",
                "id": "GO:0045540",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045540",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z6J2",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z6J2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SREBP signaling pathway",
                "id": "GO:0032933",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032933",
                "evidence": [
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                "name": "serine-type endopeptidase activity",
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                "name": "endoplasmic reticulum membrane",
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                    }
                ],
                "pmid": ""
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        ],
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                "name": "sphingolipid biosynthetic process",
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                "pmid": ""
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            {
                "name": "fatty acid elongation",
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                "name": "fatty acid elongation, monounsaturated fatty acid",
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                "name": "fatty acid elongation, polyunsaturated fatty acid",
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                "name": "fatty acid elongation, saturated fatty acid",
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                "name": "very long-chain fatty acid biosynthetic process",
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                "name": "tubulin-glutamic acid ligase activity",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
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                ],
                "pmid": ""
            },
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                "name": "ciliary basal body",
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        ],
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            {
                "name": "microtubule bundle formation",
                "id": "GO:0001578",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZBN5",
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    {
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                ],
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                ],
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                "disease_id": "DOID:3082",
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                "name": "ATPase-coupled transmembrane transporter activity",
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                ],
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            },
            {
                "name": "ATP hydrolysis activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
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                ],
                "pmid": ""
            },
            {
                "name": "ABC-type transporter activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140359",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
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        ],
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                "name": "lipid transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006869",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "membrane",
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                "pmid": ""
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        "uniprot_canonical_ac": "A1ZBT2-1",
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                ],
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        ],
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    {
        "uniprot_canonical_ac": "A1ZBU8-1",
        "species": [
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
        "length": 245,
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        "gene_names": "Bbd;Bbd;CG18067;CT40493;Dmel\\CG18067;Dmel_CG18067;bbd",
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        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBU8",
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                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBU8",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBU8"
                    }
                ],
                "pmid": ""
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        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A1ZBX9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBX9",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
        "length": 149,
        "chemical_mass": 17627.0,
        "gene_names": "Dmel\\CG13437;CG13437;Dmel\\CG13437;Dmel_CG13437",
        "protein_name": "",
        "disease": [],
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        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "A1ZBY4-1",
        "species": [
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                "name": "Drosophila melanogaster",
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                        "id": "A1ZBY4",
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                ],
                "common_name": "Fruit fly",
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        ],
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        "chemical_mass": 47498.0,
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        "protein_name": "RING-CH-type domain-containing protein",
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            {
                "name": "endosome",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005768",
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                    {
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                "pmid": ""
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            {
                "name": "membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
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                "name": "lysosome",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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            {
                "name": "ubiquitin protein ligase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061630",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin-protein transferase activity",
                "id": "GO:0004842",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004842",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY4",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein ubiquitination",
                "id": "GO:0016567",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016567",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY4",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein polyubiquitination",
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                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "vesicle-mediated transport",
                "id": "GO:0016192",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016192",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "B7Z0M0",
                        "url": "https://www.uniprot.org/uniprotkb/B7Z0M0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "SNAP receptor activity",
                "id": "GO:0005484",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005484",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2802,
        "chemical_mass": 317249.0,
        "gene_names": "Nf1;CG8318;Dmel\\CG8318;Dmel_CG8318;FBpp0084326;NF-1;NF1;Nf-1;Nf1;dNF1;dNf1;nf1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050458",
                "name": "juvenile myelomonocytic leukemia",
                "description": "A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes.",
                "url": "https://disease-ontology.org/term/DOID:0050458",
                "evidence": [
                    {
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050458"
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                ],
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            },
            {
                "disease_id": "DOID:0070482",
                "name": "spinal neurofibromatosis",
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                "url": "https://disease-ontology.org/term/DOID:0070482",
                "evidence": [
                    {
                        "id": "0070482",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070482"
                    }
                ],
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            },
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                "name": "Watson syndrome",
                "description": "A RASopathy characterized by pulmonic stenosis, cafe-au-lait macules, decreased intellectual ability, and short stature that has_material_basis_in heterozygous mutation in the NF1 gene on chromosome 17q11.2.",
                "url": "https://disease-ontology.org/term/DOID:0070483",
                "evidence": [
                    {
                        "id": "0070483",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070483"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0080199",
                "name": "colorectal carcinoma",
                "description": "A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa.",
                "url": "https://disease-ontology.org/term/DOID:0080199",
                "evidence": [
                    {
                        "id": "0080199",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080199"
                    }
                ],
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            },
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                "name": "neurofibromatosis 1",
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                "url": "https://disease-ontology.org/term/DOID:0111253",
                "evidence": [
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                        "id": "0111253",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111253"
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                ],
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            },
            {
                "disease_id": "DOID:0111683",
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                "url": "https://disease-ontology.org/term/DOID:0111683",
                "evidence": [
                    {
                        "id": "0111683",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111683"
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            },
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                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
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            },
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                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
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            },
            {
                "disease_id": "DOID:12849",
                "name": "autistic disorder",
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                "url": "https://disease-ontology.org/term/DOID:12849",
                "evidence": [
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                        "id": "12849",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12849"
                    }
                ],
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            },
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                "name": "colon cancer",
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                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3069",
                "name": "malignant astrocytoma",
                "description": "A malignant glioma that is has_material_basis_in astrocyte cells, a type of star-shaped glial cell, located in the brain and spinal cord.",
                "url": "https://disease-ontology.org/term/DOID:3069",
                "evidence": [
                    {
                        "id": "3069",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3069"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
                    {
                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
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            },
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                "disease_id": "DOID:4992",
                "name": "optic nerve glioma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:4992",
                "evidence": [
                    {
                        "id": "4992",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4992"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5151",
                "name": "plexiform neurofibroma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5151",
                "evidence": [
                    {
                        "id": "5151",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5151"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:535",
                "name": "sleep disorder",
                "description": "A disease of mental health that involves disruption of sleep patterns.",
                "url": "https://disease-ontology.org/term/DOID:535",
                "evidence": [
                    {
                        "id": "535",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:535"
                    }
                ],
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            },
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                "name": "neurofibromatosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8712",
                "evidence": [
                    {
                        "id": "8712",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8712"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9119",
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                "description": "A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.",
                "url": "https://disease-ontology.org/term/DOID:9119",
                "evidence": [
                    {
                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "response to oxidative stress",
                "id": "GO:0006979",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006979",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "adult locomotory behavior",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008344",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of multicellular organism growth",
                "id": "GO:0040014",
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                        "id": "Q9VBJ2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "short-term memory",
                "id": "GO:0007614",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007614",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
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                        "id": "Q9VBJ2",
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                    }
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                "pmid": ""
            },
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008355",
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                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotor rhythm",
                "id": "GO:0045475",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045475",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
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                "name": "response to heat",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of multicellular organism growth",
                "id": "GO:0040018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040018",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of Ras protein signal transduction",
                "id": "GO:0046578",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046578",
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perineurial glial growth",
                "id": "GO:0042066",
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                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
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                "name": "negative regulation of synaptic assembly at neuromuscular junction",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045886",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of circadian rhythm",
                "id": "GO:0042752",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042752",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of intracellular signal transduction",
                "id": "GO:1902531",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902531",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VBJ2-1",
                "start_pos": "1617",
                "end_pos": "1617",
                "site_lbl": "Thr1617",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "T",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 1617,
                        "start_aa": "Thr",
                        "end_pos": 1617,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1617",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "Q9VBJ2",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9VBJ2"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9VBJ2-1",
                "start_pos": "1791",
                "end_pos": "1791",
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                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1791,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1791",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q0KHY7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 509,
        "chemical_mass": 59032.0,
        "gene_names": "Dmel\\CG15539;CG15539-NE4;CG15539;Dmel\\CG15539;Dmel_CG15539",
        "protein_name": "procollagen-proline 4-dioxygenase",
        "disease": [],
        "molecular_function": [
            {
                "name": "iron ion binding",
                "id": "GO:0005506",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005506",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "L-ascorbic acid binding",
                "id": "GO:0031418",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031418",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "procollagen-proline 4-dioxygenase activity",
                "id": "GO:0004656",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004656",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "endoplasmic reticulum lumen",
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                        "site_lbl": "Thr250",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "H9XVM9",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=H9XVM9"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "H9XVM9-1",
                "start_pos": "55",
                "end_pos": "55",
                "site_lbl": "Ser55",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "S",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 55,
                        "start_aa": "Ser",
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                        "end_aa": "Ser",
                        "residue": "Ser",
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                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "H9XVM9",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=H9XVM9"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9NGY4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NGY4",
                        "url": "https://www.uniprot.org/uniprotkb/M9NGY4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1885,
        "chemical_mass": 205249.0,
        "gene_names": "ZAP3;CG12646;CG12647;CG2971;CG32685;Dmel\\CG32685;Dmel_CG32685;ZAP3;Zap3",
        "protein_name": "YLP motif-containing protein 1",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NGY4",
                        "url": "https://www.uniprot.org/uniprotkb/M9NGY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear speck",
                "id": "GO:0016607",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016607",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NGY4",
                        "url": "https://www.uniprot.org/uniprotkb/M9NGY4"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "protein phosphatase 1 binding",
                "id": "GO:0008157",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008157",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NGY4",
                        "url": "https://www.uniprot.org/uniprotkb/M9NGY4"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
            {
                "name": "regulation of telomere maintenance",
                "id": "GO:0032204",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032204",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "M9NGY4-1",
                "start_pos": "149",
                "end_pos": "149",
                "site_lbl": "Thr149",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 149,
                        "start_aa": "Thr",
                        "end_pos": 149,
                        "end_aa": "Thr",
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                            {
                                "id": "GLY_001163",
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                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "M9NGY4-1",
                "start_pos": "14",
                "end_pos": "14",
                "site_lbl": "Thr14",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
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                            }
                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 14,
                        "start_aa": "Thr",
                        "end_pos": 14,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr14",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "M9NGY4-1",
                "start_pos": "820",
                "end_pos": "820",
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                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
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                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 820,
                        "start_aa": "Thr",
                        "end_pos": 820,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr820",
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                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q7KTF8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 523,
        "chemical_mass": 59093.0,
        "gene_names": "nAChRalpha6;AChRalpha6;BcDNA:GH01410;CG4128;CT13662;Dalpha6;Dmel\\CG4128;Dmel_CG4128;alpha6;dalpha6;das;nACRalpha-30D;nAChR alpha 6;nAChR-alpha30D;nAChRAlpha-30D;nAChRalpha-30D;nAChRalpha6;nAChRalpha;nAChR;nAChralpha6;nAcR-alpha-30D;nAcRalpha-30D;nAchR_alpha6;rsn",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
                    {
                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12217",
                "name": "Lewy body dementia",
                "description": "A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities that has_material_basis_in accumulation of alpha-synuclein, SCNA, (protein). The causal mutation might be in SCNA or SCNB or some other gene(s) but the end result is always accumulation of SCNA in Lewy bodies.",
                "url": "https://disease-ontology.org/term/DOID:12217",
                "evidence": [
                    {
                        "id": "12217",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12217"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1561",
                "name": "cognitive disorder",
                "description": "A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.",
                "url": "https://disease-ontology.org/term/DOID:1561",
                "evidence": [
                    {
                        "id": "1561",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1561"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
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                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7148",
                "name": "rheumatoid arthritis",
                "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:7148",
                "evidence": [
                    {
                        "id": "7148",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7148"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7474",
                "name": "malignant pleural mesothelioma",
                "description": "A pleural cancer that has_material_basis_in mesothelium cells.",
                "url": "https://disease-ontology.org/term/DOID:7474",
                "evidence": [
                    {
                        "id": "7474",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7474"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8577",
                "name": "ulcerative colitis",
                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
                    {
                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
                "description": "An intestinal disease that involves inflammation located_in intestine.",
                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane signaling receptor activity",
                "id": "GO:0004888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "acetylcholine-gated monoatomic cation-selective channel activity",
                "id": "GO:0022848",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022848",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
                "id": "GO:1904315",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904315",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "excitatory extracellular ligand-gated monoatomic ion channel activity",
                "id": "GO:0005231",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005231",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "acetylcholine-gated channel complex",
                "id": "GO:0005892",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005892",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynaptic membrane",
                "id": "GO:0045211",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045211",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse",
                "id": "GO:0045202",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045202",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection",
                "id": "GO:0043005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "muscle cell cellular homeostasis",
                "id": "GO:0046716",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046716",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation transport",
                "id": "GO:0006812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic transmission, cholinergic",
                "id": "GO:0007271",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007271",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of membrane potential",
                "id": "GO:0042391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic ion transmembrane transport",
                "id": "GO:0034220",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034220",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KTF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KTF8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q7KTF8-1",
                "start_pos": "392",
                "end_pos": "392",
                "site_lbl": "Thr392",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "T",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 392,
                        "start_aa": "Thr",
                        "end_pos": 392,
                        "end_aa": "Thr",
                        "residue": "Thr",
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        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1096,
        "chemical_mass": 123282.0,
        "gene_names": "Eph;CG1511;CT3831;DEK;Dek7;Dek;Deph;Dmel\\CG1511;Dmel_CG1511;EPH;Ek7;Eph;RPTK Dek7;dek;eph;lincRNA.923",
        "protein_name": "receptor protein-tyrosine kinase",
        "disease": [
            {
                "disease_id": "DOID:0070611",
                "name": "autosomal dominant nonsyndromic deafness 88",
                "description": "An autosomal dominant nonsyndromic deafness characterized by postlingual progressive severe sensorineural hearing loss with tinnitus that has_material_basis_in heterozygous mutation in the EPHA10 gene on chromosome 1p34.",
                "url": "https://disease-ontology.org/term/DOID:0070611",
                "evidence": [
                    {
                        "id": "0070611",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070611"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080685",
                "name": "aortic dissection",
                "description": "An aortic disease that is characterized by tearing of the intimal layer of the aorta resulting in separation of the layers of the aortic wall.",
                "url": "https://disease-ontology.org/term/DOID:0080685",
                "evidence": [
                    {
                        "id": "0080685",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080685"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081030",
                "name": "central conducting lymphatic anomaly",
                "description": "A lymphatic system disease that is characterized by dysfunction of the thoracic duct or cisterna chyli, leading to a retrograde flux of lymphatic fluid or abnormal drainage of lymphatic fluid and that has_material_basis_in heterozygous mutation in the EPHB4 gene on chromosome 7q22.",
                "url": "https://disease-ontology.org/term/DOID:0081030",
                "evidence": [
                    {
                        "id": "0081030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110229",
                "name": "cataract 6 multiple types",
                "description": "A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36.",
                "url": "https://disease-ontology.org/term/DOID:0110229",
                "evidence": [
                    {
                        "id": "0110229",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110229"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12365",
                "name": "malaria",
                "description": "A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle.",
                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
                        "id": "12365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1561",
                "name": "cognitive disorder",
                "description": "A disease of mental health that affects cognitive functions including memory processing, perception and problem solving.",
                "url": "https://disease-ontology.org/term/DOID:1561",
                "evidence": [
                    {
                        "id": "1561",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1561"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2218",
                "name": "blood platelet disease",
                "description": "A blood coagulation disease that is characterized by an abnormal increase or decrease in platelets or platelet dysfunction.",
                "url": "https://disease-ontology.org/term/DOID:2218",
                "evidence": [
                    {
                        "id": "2218",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2218"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:264",
                "name": "hemangiopericytoma",
                "description": "A hemangiopericytic tumor that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries.",
                "url": "https://disease-ontology.org/term/DOID:264",
                "evidence": [
                    {
                        "id": "264",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:264"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2975",
                "name": "cystic kidney disease",
                "description": "A kidney disease that is characterized by the formation of cysts (fluid-filled sacs) in and around the kidney.",
                "url": "https://disease-ontology.org/term/DOID:2975",
                "evidence": [
                    {
                        "id": "2975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2975"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3525",
                "name": "middle cerebral artery infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3525",
                "evidence": [
                    {
                        "id": "3525",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3525"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3602",
                "name": "toxic encephalopathy",
                "description": "A nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems.",
                "url": "https://disease-ontology.org/term/DOID:3602",
                "evidence": [
                    {
                        "id": "3602",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3602"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:75",
                "name": "lymphatic system disease",
                "description": "An immune system disease that is located_in the lymphatic system.",
                "url": "https://disease-ontology.org/term/DOID:75",
                "evidence": [
                    {
                        "id": "75",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:75"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8577",
                "name": "ulcerative colitis",
                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
                    {
                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9778",
                "name": "irritable bowel syndrome",
                "description": "An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause.",
                "url": "https://disease-ontology.org/term/DOID:9778",
                "evidence": [
                    {
                        "id": "9778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane-ephrin receptor activity",
                "id": "GO:0005005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane receptor protein tyrosine kinase activity",
                "id": "GO:0004714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "receptor complex",
                "id": "GO:0043235",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043235",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ephrin receptor signaling pathway",
                "id": "GO:0048013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mushroom body development",
                "id": "GO:0016319",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016319",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "melanotic encapsulation of foreign target",
                "id": "GO:0035011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell surface receptor protein tyrosine kinase signaling pathway",
                "id": "GO:0007169",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007169",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V4E5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V4E5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8IPH8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2122,
        "chemical_mass": 243303.0,
        "gene_names": "Myo28B1;28B;CG6976;DmVIIB;Dmel\\CG6976;Dmel_CG6976;Myo18;Myo28B1;Myo28B;VIIb 28B;myo 28B1;myo28B",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "system development",
                "id": "GO:0048731",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048731",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament-based movement",
                "id": "GO:0030048",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030048",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tissue development",
                "id": "GO:0009888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "animal organ development",
                "id": "GO:0048513",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048513",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "animal organ morphogenesis",
                "id": "GO:0009887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron differentiation",
                "id": "GO:0030182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament organization",
                "id": "GO:0007015",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007015",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory organ development",
                "id": "GO:0007423",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007423",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "actin binding",
                "id": "GO:0003779",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microfilament motor activity",
                "id": "GO:0000146",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000146",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament binding",
                "id": "GO:0051015",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051015",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IPH8",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IPH8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myosin complex",
                "id": "GO:0016459",
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            {
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            {
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                        "url": "https://www.alliancegenome.org/disease/DOID:13413"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1824",
                "name": "status epilepticus",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1824",
                "evidence": [
                    {
                        "id": "1824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2560",
                "name": "morphine dependence",
                "description": "An opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:2560",
                "evidence": [
                    {
                        "id": "2560",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2560"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5418",
                "name": "schizoaffective disorder",
                "description": "A psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality.",
                "url": "https://disease-ontology.org/term/DOID:5418",
                "evidence": [
                    {
                        "id": "5418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:670",
                "name": "amphetamine abuse",
                "description": "A substance abuse that involves the recurring use of amphetamines despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:670",
                "evidence": [
                    {
                        "id": "670",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:670"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:809",
                "name": "cocaine abuse",
                "description": "A substance abuse that involves the recurring use of cocaine despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:809",
                "evidence": [
                    {
                        "id": "809",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:809"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9279",
                "name": "hyperhomocysteinemia",
                "description": "An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood.",
                "url": "https://disease-ontology.org/term/DOID:9279",
                "evidence": [
                    {
                        "id": "9279",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9279"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9505",
                "name": "cannabis abuse",
                "description": "A substance abuse that involves the recurring use of cannabis despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:9505",
                "evidence": [
                    {
                        "id": "9505",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9505"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9976",
                "name": "heroin dependence",
                "description": "An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9976",
                "evidence": [
                    {
                        "id": "9976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "transmitter-gated monoatomic ion channel activity",
                "id": "GO:0022824",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022824",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular ligand-gated monoatomic ion channel activity",
                "id": "GO:0005230",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005230",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
                "id": "GO:1904315",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904315",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glutamate receptor activity",
                "id": "GO:0008066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "ionotropic glutamate receptor complex",
                "id": "GO:0008328",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008328",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynaptic membrane",
                "id": "GO:0045211",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045211",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynaptic density membrane",
                "id": "GO:0098839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell surface receptor signaling pathway",
                "id": "GO:0007166",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007166",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation transport",
                "id": "GO:0006812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic transmission, glutamatergic",
                "id": "GO:0035249",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035249",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "modulation of chemical synaptic transmission",
                "id": "GO:0050804",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050804",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHV5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "M9PHV5-1",
                "start_pos": "703",
                "end_pos": "703",
                "site_lbl": "Thr703",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 703,
                        "start_aa": "Thr",
                        "end_pos": 703,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr703",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8IQE6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1076,
        "chemical_mass": 120321.0,
        "gene_names": "IRSp53;CG32082;CG7624;Dmel\\CG32082;Dmel_CG32082;IRSp53;IRS;anon-WO0118547.199",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1094",
                "name": "attention deficit hyperactivity disorder",
                "description": "A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age.",
                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11119",
                "name": "Gilles de la Tourette syndrome",
                "description": "A tic disorder that is characterized by multiple physical (motor) tics and at least one vocal (phonic) tic present for more than a year.",
                "url": "https://disease-ontology.org/term/DOID:11119",
                "evidence": [
                    {
                        "id": "11119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11119"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "phospholipid binding",
                "id": "GO:0005543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "plasma membrane organization",
                "id": "GO:0007009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "filopodium assembly",
                "id": "GO:0046847",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046847",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane organization",
                "id": "GO:0061024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061024",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament bundle assembly",
                "id": "GO:0051017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin crosslink formation",
                "id": "GO:0051764",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051764",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of actin filament polymerization",
                "id": "GO:0030838",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030838",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IQE6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IQE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "E1JIZ4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 624,
        "chemical_mass": 69489.0,
        "gene_names": "Men-b;CG5889;Dmel\\CG5889;Dmel_CG5889;MDH;Mdh;Men-B;Men-b;anon-EST:Posey79;dME-3;dME3",
        "protein_name": "Malic enzyme",
        "disease": [],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NAD binding",
                "id": "GO:0051287",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051287",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "malate dehydrogenase (decarboxylating) (NADP+) activity",
                "id": "GO:0004473",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004473",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "malate metabolic process",
                "id": "GO:0006108",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006108",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIZ4",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIZ4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q59DP4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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            },
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                "name": "regulation of calcium ion transport into cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010522",
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                ],
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            {
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            {
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                "name": "protein homodimerization activity",
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            {
                "name": "protein heterodimerization activity",
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        "gene_names": "Dmel\\CG17707;CG17707;Dmel\\CG17707;Dmel_CG17707;EG:23E12.3",
        "protein_name": "Nose resistant-to-fluoxetine protein N-terminal domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "acyltransferase activity, transferring groups other than amino-acyl groups",
                "id": "GO:0016747",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016747",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUS7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUS7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
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        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 542,
        "chemical_mass": 58408.0,
        "gene_names": "zyd;BEST:CK02262;CG2893;CG40147;CK02262;Dmel\\CG2893;Dmel_CG2893;Nckx-x;Ncxk-x;zyd",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110063",
                "name": "amelogenesis imperfecta hypomaturation type 2A5",
                "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.",
                "url": "https://disease-ontology.org/term/DOID:0110063",
                "evidence": [
                    {
                        "id": "0110063",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110063"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10123",
                "name": "pigmentation disease",
                "description": "A skin disease that is characterized by discoloration of the skin.",
                "url": "https://disease-ontology.org/term/DOID:10123",
                "evidence": [
                    {
                        "id": "10123",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10123"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "calcium ion transport",
                "id": "GO:0006816",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006816",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "potassium ion transport",
                "id": "GO:0006813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transport",
                "id": "GO:0006814",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium-mediated signaling",
                "id": "GO:0019722",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019722",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular calcium ion homeostasis",
                "id": "GO:0006874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transmembrane transport",
                "id": "GO:0070588",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070588",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "symporter activity",
                "id": "GO:0015293",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015293",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "antiporter activity",
                "id": "GO:0015297",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015297",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium channel activity",
                "id": "GO:0005262",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005262",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium, potassium:sodium antiporter activity",
                "id": "GO:0008273",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008273",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5LJX8",
                        "url": "https://www.uniprot.org/uniprotkb/Q5LJX8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q5LJX8-1",
                "start_pos": "158",
                "end_pos": "158",
                "site_lbl": "Thr158",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 158,
                        "start_aa": "Thr",
                        "end_pos": 158,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr158",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VAJ0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 254,
        "chemical_mass": 28582.0,
        "gene_names": "Dmel\\CG7582;CG7582;Dmel\\CG7582;Dmel_CG7582",
        "protein_name": "lysoplasmalogenase",
        "disease": [],
        "molecular_function": [
            {
                "name": "alkenylglycerophosphocholine hydrolase activity",
                "id": "GO:0047408",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047408",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAJ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAJ0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q3KN41-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1840,
        "chemical_mass": 199615.0,
        "gene_names": "Nrx-1;CG7050;CT21808;DNrx;Dmel\\CG7050;Dmel_CG7050;Dnrx;Nrx-1;Nrx-I;Nrx1;Nrx;dNRXN3;dNrx;dnrx-1;dnrx1;dnrx;neurexin;nrx-1;nrx1;nrx",
        "protein_name": "Neurexin 1",
        "disease": [
            {
                "disease_id": "DOID:0050741",
                "name": "alcohol dependence",
                "description": "A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0050741",
                "evidence": [
                    {
                        "id": "0050741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
                    {
                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111332",
                "name": "Pitt-Hopkins-like syndrome 2",
                "description": "A syndromic intellectual disability characterized by developmental delay and intellectual disability with many patients also displaying infantile hypotonia and autistic features that has_material_basis_in compound heterozygous or homozygous mutation in the NRXN1 gene on chromosome 2p16.3.",
                "url": "https://disease-ontology.org/term/DOID:0111332",
                "evidence": [
                    {
                        "id": "0111332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "neuromuscular synaptic transmission",
                "id": "GO:0007274",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007274",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "associative learning",
                "id": "GO:0008306",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008306",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse organization",
                "id": "GO:0050808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic assembly at neuromuscular junction",
                "id": "GO:0051124",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051124",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chemical synaptic transmission",
                "id": "GO:0007268",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007268",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse assembly",
                "id": "GO:0007416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotion",
                "id": "GO:0040011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic vesicle endocytosis",
                "id": "GO:0048488",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048488",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuroligin clustering involved in postsynaptic membrane assembly",
                "id": "GO:0097118",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097118",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "vitamin A transport",
                "id": "GO:0071938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071938",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "gephyrin clustering involved in postsynaptic density assembly",
                "id": "GO:0097116",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097116",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "learning",
                "id": "GO:0007612",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007612",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adult behavior",
                "id": "GO:0030534",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030534",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "terminal button organization",
                "id": "GO:0072553",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072553",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of terminal button organization",
                "id": "GO:2000331",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000331",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "presynaptic membrane assembly",
                "id": "GO:0097105",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097105",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "neuromuscular junction",
                "id": "GO:0031594",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031594",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q3KN41",
                        "url": "https://www.uniprot.org/uniprotkb/Q3KN41"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "terminal bouton",
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                "name": "mesoderm migration involved in gastrulation",
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                    }
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                "pmid": ""
            },
            {
                "name": "pericardial nephrocyte differentiation",
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                "pmid": ""
            }
        ],
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            {
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                "id": "GO:0005615",
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            }
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                "pmid": ""
            },
            {
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                "id": "GO:0048018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048018",
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                "pmid": ""
            },
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                "name": "fibroblast growth factor receptor binding",
                "id": "GO:0005104",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005104",
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                ],
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            }
        ],
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        ],
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                    }
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        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
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                        "id": "Q0E910",
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                ],
                "pmid": ""
            },
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                "name": "perinuclear region of cytoplasm",
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                    }
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                "pmid": ""
            },
            {
                "name": "P granule",
                "id": "GO:0043186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043186",
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                        "id": "Q0E910",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "spermatogenesis",
                "id": "GO:0007283",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
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                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E910"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "secondary piRNA processing",
                "id": "GO:0140965",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140965",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E910"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transposable element silencing by piRNA-mediated mRNA destabilization",
                "id": "GO:0141009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0141009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0E910",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E910"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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            {
                "uniprot_canonical_ac": "Q0E910-1",
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                "end_pos": "328",
                "site_lbl": "Thr328",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "end_aa": "Thr",
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                        "site_lbl": "Thr328",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
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                            }
                        ]
                    }
                ]
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            {
                "uniprot_canonical_ac": "Q0E910-1",
                "start_pos": "335",
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                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                            }
                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
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                        "comment": "",
                        "icn3d_view": {},
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                        "start_aa": "Thr",
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                        "end_aa": "Thr",
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                        "site_lbl": "Thr335",
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                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "E1JGT2-1",
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            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JGT2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JGT2"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 8757.0,
        "gene_names": "Dmel\\CG44253;CG30194;CG44253;Dmel\\CG44253;Dmel_CG44253",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q59DZ7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q59DZ7"
                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 116547.0,
        "gene_names": "Ddr;CG11573;CG13985;CG33531;CG9488;CG9490;CT33540;DDR;Ddr;Dmel\\CG33531;Dmel_CG33531;ddr",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
                "description": "An oral cavity cancer that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:0050866",
                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0112196",
                "name": "spondylometaepiphyseal dysplasia, short limb-hand type",
                "description": "A spondyloepimetaphyseal dysplasia characterized by short stature, short limbs and hands, and typical radiological features which include platyspondyly, metaphyseal, and epiphyseal involvement, short tubular bones of the limbs, and abnormal calcification of cartilage that has_material_basis_in homozygous or compound heterozygous mutation in the DDR2 gene on chromosome 1q23.3.",
                "url": "https://disease-ontology.org/term/DOID:0112196",
                "evidence": [
                    {
                        "id": "0112196",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112196"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
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            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
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            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
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            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
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                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
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                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
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            },
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                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
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                "disease_id": "DOID:3347",
                "name": "osteosarcoma",
                "description": "A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus).",
                "url": "https://disease-ontology.org/term/DOID:3347",
                "evidence": [
                    {
                        "id": "3347",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3347"
                    }
                ],
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            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3500",
                "name": "gallbladder adenocarcinoma",
                "description": "A gallbladder carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3500",
                "evidence": [
                    {
                        "id": "3500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3500"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3907",
                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.",
                "url": "https://disease-ontology.org/term/DOID:3907",
                "evidence": [
                    {
                        "id": "3907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3907"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4467",
                "name": "clear cell renal cell carcinoma",
                "description": "A renal cell carcinoma that has_material_basis_in cells that appear very pale or clear when examined under microscope.",
                "url": "https://disease-ontology.org/term/DOID:4467",
                "evidence": [
                    {
                        "id": "4467",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4467"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5520",
                "name": "head and neck squamous cell carcinoma",
                "description": "A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck.",
                "url": "https://disease-ontology.org/term/DOID:5520",
                "evidence": [
                    {
                        "id": "5520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5520"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5627",
                "name": "adenosquamous gallbladder carcinoma",
                "description": "A gallbladder carcinoma that derives_from squamous cells and gland-like cells.",
                "url": "https://disease-ontology.org/term/DOID:5627",
                "evidence": [
                    {
                        "id": "5627",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5627"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8398",
                "name": "osteoarthritis",
                "description": "An arthritis that has_material_basis_in worn out cartilage located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:8398",
                "evidence": [
                    {
                        "id": "8398",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8398"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8923",
                "name": "skin melanoma",
                "description": "A skin cancer that has_material_basis_in melanocytes.",
                "url": "https://disease-ontology.org/term/DOID:8923",
                "evidence": [
                    {
                        "id": "8923",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8923"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9261",
                "name": "nasopharynx carcinoma",
                "description": "A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract.",
                "url": "https://disease-ontology.org/term/DOID:9261",
                "evidence": [
                    {
                        "id": "9261",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9261"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q59DZ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane receptor protein tyrosine kinase activity",
                "id": "GO:0004714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q59DZ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "collagen binding",
                "id": "GO:0005518",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005518",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q59DZ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein tyrosine kinase collagen receptor activity",
                "id": "GO:0038062",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0038062",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q59DZ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q59DZ7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
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    {
        "uniprot_canonical_ac": "E1JJF2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJF2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJF2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 385,
        "chemical_mass": 44985.0,
        "gene_names": "Dmel\\CG4558;CG4558;Dmel\\CG4558;Dmel_CG4558",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJF2",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJF2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "E2QCM9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 476,
        "chemical_mass": 54061.0,
        "gene_names": "Dh44-R2;CG12370;CG13156;DH-R;DH44-R2;DH44R2;DH[[44]]-R2;Dh44-R2;Dh442;Dh44R2;Dmel\\CG12370;Dmel_CG12370;anon-WO0170980.103;anon-WO0170980.104",
        "protein_name": "Diuretic hormone receptor",
        "disease": [
            {
                "disease_id": "DOID:0050696",
                "name": "fetal alcohol spectrum disorder",
                "description": "A specific developmental disorder and physical disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of alcohol during pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:0050696",
                "evidence": [
                    {
                        "id": "0050696",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050696"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12918",
                "name": "thromboangiitis obliterans",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12918",
                "evidence": [
                    {
                        "id": "12918",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12918"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3877",
                "name": "functional colonic disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3877",
                "evidence": [
                    {
                        "id": "3877",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3877"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4483",
                "name": "rhinitis",
                "description": "A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip.",
                "url": "https://disease-ontology.org/term/DOID:4483",
                "evidence": [
                    {
                        "id": "4483",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4483"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9778",
                "name": "irritable bowel syndrome",
                "description": "An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause.",
                "url": "https://disease-ontology.org/term/DOID:9778",
                "evidence": [
                    {
                        "id": "9778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9778"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9976",
                "name": "heroin dependence",
                "description": "An opiate dependence that involves the continued use of heroin despite problems related to use of the substance.",
                "url": "https://disease-ontology.org/term/DOID:9976",
                "evidence": [
                    {
                        "id": "9976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell surface receptor signaling pathway",
                "id": "GO:0007166",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007166",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "G protein-coupled receptor signaling pathway",
                "id": "GO:0007186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007186",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-modulating G protein-coupled receptor signaling pathway",
                "id": "GO:0007188",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007188",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hormone-mediated signaling pathway",
                "id": "GO:0009755",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009755",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to salt stress",
                "id": "GO:0009651",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009651",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "peptide hormone binding",
                "id": "GO:0017046",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017046",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "G protein-coupled peptide receptor activity",
                "id": "GO:0008528",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008528",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcitonin receptor activity",
                "id": "GO:0004948",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004948",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuropeptide receptor activity",
                "id": "GO:0008188",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008188",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "diuretic hormone receptor activity",
                "id": "GO:0008036",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008036",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E2QCM9",
                        "url": "https://www.uniprot.org/uniprotkb/E2QCM9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9V491-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1945,
        "chemical_mass": 218358.0,
        "gene_names": "PlexA;BcDNA:GM05237;CG11081;D-Plex A;DPlexA;Dmel\\CG11081;Dmel_CG11081;Plex1;PlexA1;PlexA;Plexa;PlexinA;lincRNA.927;plex A;plexA;plex",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heparin binding",
                "id": "GO:0008201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "14-3-3 protein binding",
                "id": "GO:0071889",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071889",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "semaphorin receptor activity",
                "id": "GO:0017154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "guanylate cyclase activator activity",
                "id": "GO:0030250",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030250",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "semaphorin receptor complex",
                "id": "GO:0002116",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002116",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "axon midline choice point recognition",
                "id": "GO:0016199",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016199",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Ras protein signal transduction",
                "id": "GO:0007265",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007265",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory neuron axon guidance",
                "id": "GO:0097374",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097374",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "semaphorin-plexin signaling pathway",
                "id": "GO:0071526",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071526",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse assembly",
                "id": "GO:0007416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell migration",
                "id": "GO:0030334",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030334",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "photoreceptor cell axon guidance",
                "id": "GO:0072499",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072499",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V491",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V491"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9V491-1",
                "start_pos": "114",
                "end_pos": "114",
                "site_lbl": "Asn114",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "N-linked",
                        "subtype": "",
                        "prediction_tool_list": [],
                        "site_category": "reported",
                        "site_category_dict": {
                            "reported": true
                        },
                        "site_seq": "N",
                        "relation": "attached",
                        "comment": "N-linked (GlcNAc...) asparagine",
                        "icn3d_view": {},
                        "start_pos": 114,
                        "start_aa": "Asn",
                        "end_pos": 114,
                        "end_aa": "Asn",
                        "residue": "Asn",
                        "site_lbl": "Asn114",
                        "evidence": [
                            {
                                "id": "Q9V491",
                                "database": "UniProtKB",
                                "url": "https://www.uniprot.org/uniprotkb/Q9V491#ptm_processing"
                            },
                            {
                                "id": "6FKM",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/sequence/6FKM"
                            },
                            {
                                "id": "6FKN",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/sequence/6FKN"
                            },
                            {
                                "id": "6FKM",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/structure/6FKM"
                            },
                            {
                                "id": "6FKM",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/structure/6FKM"
                            },
                            {
                                "id": "6FKN",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/structure/6FKN"
                            },
                            {
                                "id": "6FKN",
                                "database": "PDB",
                                "url": "https://www.rcsb.org/structure/6FKN"
                            },
                            {
                                "id": "6FKM|A|114",
                                "database": "",
                                "url": ""
                            },
                            {
                                "id": "6FKN|C|114",
                                "database": "",
                                "url": ""
                            },
                            {
                                "id": "6FKN|A|114",
                                "database": "",
                                "url": ""
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                        ]
                    }
                ]
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                            {
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                            {
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                            },
                            {
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                            {
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                                "database": "",
                                "url": ""
                            },
                            {
                                "id": "6FKN|C|167",
                                "database": "",
                                "url": ""
                            },
                            {
                                "id": "6FKN|A|167",
                                "database": "",
                                "url": ""
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                        ]
                    }
                ]
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            {
                "uniprot_canonical_ac": "Q9V491-1",
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                "site_lbl": "Asn185",
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                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                        "site_category_dict": {
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                        "relation": "attached",
                        "comment": "N-linked (GlcNAc...) asparagine",
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                        "start_aa": "Asn",
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                        "end_aa": "Asn",
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                            {
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                            {
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                            {
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                            {
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                            },
                            {
                                "id": "6FKN",
                                "database": "PDB",
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                            },
                            {
                                "id": "6FKM|A|185",
                                "database": "",
                                "url": ""
                            },
                            {
                                "id": "6FKN|C|185",
                                "database": "",
                                "url": ""
                            },
                            {
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                                "database": "",
                                "url": ""
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                        ]
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                ]
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            {
                "uniprot_canonical_ac": "Q9V491-1",
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                    {
                        "glytoucan_ac": "",
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                        "comment": "N-linked (GlcNAc...) asparagine",
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                        "start_aa": "Asn",
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                        "end_aa": "Asn",
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                            {
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                            },
                            {
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                            {
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                        ]
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                ]
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            {
                "uniprot_canonical_ac": "Q9V491-1",
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                "end_pos": "723",
                "site_lbl": "Ser723",
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                    {
                        "glytoucan_ac": "G49108TO",
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                        },
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                        "comment": "O-GlcNAcylation",
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                        "end_aa": "Ser",
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                        "site_lbl": "Ser723",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
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                            },
                            {
                                "id": "Q9V491",
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                            }
                        ]
                    }
                ]
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            {
                "uniprot_canonical_ac": "Q9V491-1",
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                    {
                        "glytoucan_ac": "",
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                            {
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                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
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                        "start_aa": "Thr",
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                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
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                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9ND53-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
        "length": 2047,
        "chemical_mass": 215083.0,
        "gene_names": "tai;2;58/2;CG13109;CG18494;DAIB1;DmTaiman;DmTai;Dmel\\CG13109;Dmel_CG13109;EP(2)2630;NEST:bs13g05;TAI;Taiman;Tai;bs13g05.y1;l(2)01351;l(2)k05802;l(2)k05809;tai",
        "protein_name": "",
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                "disease_id": "DOID:0050861",
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                "description": "A colorectal carcinoma that derives_from epithelial cells of glandular origin.",
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                        "id": "0050861",
                        "database": "AGR",
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                ],
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            },
            {
                "disease_id": "DOID:0080199",
                "name": "colorectal carcinoma",
                "description": "A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa.",
                "url": "https://disease-ontology.org/term/DOID:0080199",
                "evidence": [
                    {
                        "id": "0080199",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080199"
                    }
                ],
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            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
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                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
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                ],
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            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
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                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
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                ],
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            },
            {
                "disease_id": "DOID:11612",
                "name": "polycystic ovary syndrome",
                "description": "An ovarian dysfunction that is characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight.",
                "url": "https://disease-ontology.org/term/DOID:11612",
                "evidence": [
                    {
                        "id": "11612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11633",
                "name": "thyroid hormone resistance syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11633",
                "evidence": [
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                        "id": "11633",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11633"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
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                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
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                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
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                ],
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                ],
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                        "database": "AGR",
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                ],
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            {
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                "evidence": [
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                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
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            },
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                "evidence": [
                    {
                        "id": "7474",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7474"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9119",
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                "evidence": [
                    {
                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
                    }
                ],
                "weight": 0.0
            },
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                "url": "https://disease-ontology.org/term/DOID:9970",
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                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "transcription coactivator activity",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein dimerization activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046983",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
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                "name": "nuclear receptor binding",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coactivator binding",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription regulator inhibitor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140416",
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                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "positive regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of growth",
                "id": "GO:0045927",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045927",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "border follicle cell migration",
                "id": "GO:0007298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007298",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "germ-line stem-cell niche homeostasis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060250",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of border follicle cell migration",
                "id": "GO:1903688",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903688",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to hormone stimulus",
                "id": "GO:0032870",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032870",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of smoothened signaling pathway",
                "id": "GO:0045879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND53",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND53"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "M9ND53-1",
                "start_pos": "1492",
                "end_pos": "1492",
                "site_lbl": "Thr1492",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1492,
                        "start_aa": "Thr",
                        "end_pos": 1492,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1492",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9MRI7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9MRI7",
                        "url": "https://www.uniprot.org/uniprotkb/M9MRI7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 43,
        "chemical_mass": 5313.0,
        "gene_names": "Dmel\\CG42751;CG42751;Dmel\\CG42751;Dmel_CG42751",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8IP51-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 3375,
        "chemical_mass": 374749.0,
        "gene_names": "wb;2Lan;2]];2;A1;BEST:CK02229;BG:DS03792.1;BG:DS03792.2;CG15288;CG32970;CG42677;CK02229;CT35236;DLAM;Dmel\\CG42677;Dmel_CG42677;LM-A/alpha2;LanA1;LanWb;Wb;alpha1;alpha2;alpha[[1;fus5;l(2)09437;l(2)34Fb;l(2)br1;l34Fb;wb",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0061132",
                "name": "autosomal recessive limb-girdle muscular dystrophy type 23",
                "description": "An autosomal recessive limb-girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness primarily affecting the lower limbs and resulting in gait difficulties that has_material_basis_in y homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.",
                "url": "https://disease-ontology.org/term/DOID:0061132",
                "evidence": [
                    {
                        "id": "0061132",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061132"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110636",
                "name": "congenital merosin-deficient muscular dystrophy 1A",
                "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscle weakness that is apparent at birth or in the first 6 months of life and frequent development of periventricular white matter abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.",
                "url": "https://disease-ontology.org/term/DOID:0110636",
                "evidence": [
                    {
                        "id": "0110636",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110636"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11830",
                "name": "myopia",
                "description": "A refractive error characterized by the inability to see farther objects clearly.",
                "url": "https://disease-ontology.org/term/DOID:11830",
                "evidence": [
                    {
                        "id": "11830",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11830"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1591",
                "name": "renovascular hypertension",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1591",
                "evidence": [
                    {
                        "id": "1591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9884",
                "name": "muscular dystrophy",
                "description": "A myopathy is characterized by progressive skeletal muscle weakness degeneration.",
                "url": "https://disease-ontology.org/term/DOID:9884",
                "evidence": [
                    {
                        "id": "9884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9884"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
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                ],
                "pmid": ""
            },
            {
                "name": "gonad development",
                "id": "GO:0008406",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008406",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
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                ],
                "pmid": ""
            },
            {
                "name": "digestive tract mesoderm development",
                "id": "GO:0007502",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007502",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "animal organ morphogenesis",
                "id": "GO:0009887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tissue development",
                "id": "GO:0009888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009888",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "epithelial structure maintenance",
                "id": "GO:0010669",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010669",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "basement membrane",
                "id": "GO:0005604",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005604",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "extracellular matrix structural constituent",
                "id": "GO:0005201",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005201",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP51",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP51"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    {
        "uniprot_canonical_ac": "M9MSI4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "M9MSI4",
                        "url": "https://www.uniprot.org/uniprotkb/M9MSI4"
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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            {
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                "description": "A hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones.",
                "url": "https://disease-ontology.org/term/DOID:0060870",
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                    {
                        "id": "0060870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060870"
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0080552",
                "evidence": [
                    {
                        "id": "0080552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080552"
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                ],
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            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
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                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
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                ],
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            },
            {
                "disease_id": "DOID:3490",
                "name": "Noonan syndrome",
                "description": "A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms.",
                "url": "https://disease-ontology.org/term/DOID:3490",
                "evidence": [
                    {
                        "id": "3490",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3490"
                    }
                ],
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            },
            {
                "disease_id": "DOID:8689",
                "name": "anorexia nervosa",
                "description": "An eating disorder characterized by refusal to maintain a healthy body weight, and an obsessive fear of gaining weight due to a distorted self image.",
                "url": "https://disease-ontology.org/term/DOID:8689",
                "evidence": [
                    {
                        "id": "8689",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8689"
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                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9MSI4",
                        "url": "https://www.uniprot.org/uniprotkb/M9MSI4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    {
        "uniprot_canonical_ac": "M9MSI7-1",
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            {
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                    {
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                ],
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        ],
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        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
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    {
        "uniprot_canonical_ac": "M9NCU2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 8691.0,
        "gene_names": "Dmel\\CG43376;CG43376;Dmel\\CG43376;Dmel_CG43376",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9NDD9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "gene_names": "Dmel\\CG43165;CG43165;Dmel\\CG43165;Dmel_CG43165",
        "protein_name": "BPTI/Kunitz inhibitor domain-containing protein",
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            {
                "name": "serine-type endopeptidase inhibitor activity",
                "id": "GO:0004867",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004867",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NDD9",
                        "url": "https://www.uniprot.org/uniprotkb/M9NDD9"
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                ],
                "pmid": ""
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        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
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    {
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            {
                "name": "Drosophila melanogaster",
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                    {
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "protein_name": "Secreted protein",
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        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
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    {
        "uniprot_canonical_ac": "M9NDZ8-1",
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            {
                "name": "Drosophila melanogaster",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 20946.0,
        "gene_names": "Dmel\\CG43074;CG43074;Dmel\\CG43074;Dmel_CG43074",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9NDZ9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
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                    {
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                        "id": "M9NDZ9",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 28780.0,
        "gene_names": "Dmel\\CG43331;CG12377;CG43331;Dmel\\CG43331;Dmel_CG43331",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9PJN5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PJN5",
                        "url": "https://www.uniprot.org/uniprotkb/M9PJN5"
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 130897.0,
        "gene_names": "HDAC6;CG6170;DHDAC2;DmHDAC2;Dmel\\CG6170;Dmel_CG6170;HDAC2;HDAC6;HDAC;Hdac6;dHDAC2;dHDAC6;dmHDA404;hDAC6;hdac6",
        "protein_name": "Protein deacetylase HDAC6",
        "disease": [
            {
                "disease_id": "DOID:0060980",
                "name": "polycystic liver disease 1",
                "description": "A polycystic disease characterized by the presence of multiple liver cysts of biliary epithelial origin that has_material_basis_in heterozygous mutation in the PRKCSH gene on chromosome 19p13.",
                "url": "https://disease-ontology.org/term/DOID:0060980",
                "evidence": [
                    {
                        "id": "0060980",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060980"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0080322",
                "name": "polycystic kidney disease",
                "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure.",
                "url": "https://disease-ontology.org/term/DOID:0080322",
                "evidence": [
                    {
                        "id": "0080322",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080322"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112106",
                "name": "chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia",
                "description": "A syndrome characterized by chondrodysplasia associated with other features including intrauterine growth retardation, hydrocephaly, macrocephaly, frontal bossing, microphthalmia, small low-set ears, and short flat nose that has_material_basis_in heterozygous mutation in the HDAC6 gene on chromosome Xp11.23.",
                "url": "https://disease-ontology.org/term/DOID:0112106",
                "evidence": [
                    {
                        "id": "0112106",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112106"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4947",
                "name": "cholangiocarcinoma",
                "description": "A bile duct adenocarcinoma that has_material_basis_in bile duct epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:4947",
                "evidence": [
                    {
                        "id": "4947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8991",
                "name": "cervix uteri carcinoma in situ",
                "description": "An uterus carcinoma in situ that is located_in the uterine cervix.",
                "url": "https://disease-ontology.org/term/DOID:8991",
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                ],
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            },
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        ],
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            {
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            {
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                "pmid": ""
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            {
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                ],
                "pmid": ""
            },
            {
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                ],
                "pmid": ""
            },
            {
                "name": "actin binding",
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                "pmid": ""
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            {
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            },
            {
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                    }
                ],
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            },
            {
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
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                ],
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            },
            {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H4K8 deacetylase activity, hydrolytic mechanism",
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                ],
                "pmid": ""
            },
            {
                "name": "histone H4K12 deacetylase activity, hydrolytic mechanism",
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                    {
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                    }
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                        },
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    {
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        ],
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    },
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                ],
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        ],
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        "protein_name": "",
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            },
            {
                "name": "membrane",
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                ],
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            },
            {
                "name": "phagocytosis",
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            {
                "name": "defense response to bacterium",
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                    }
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        "protein_name": "Sphingolipid delta(4)-desaturase DES1",
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                "url": "https://disease-ontology.org/term/DOID:0070399",
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            },
            {
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                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:9970",
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                ],
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            }
        ],
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            {
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                "name": "endoplasmic reticulum",
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                ],
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            {
                "name": "endoplasmic reticulum membrane",
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                            {
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        ],
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            {
                "name": "insemination",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular space",
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                    {
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                ],
                "pmid": ""
            }
        ],
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                ],
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            {
                "name": "endoplasmic reticulum",
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                ],
                "pmid": ""
            },
            {
                "name": "membrane",
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                ],
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                ],
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        ],
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            },
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                ],
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        ],
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                "name": "calcium ion binding",
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                ],
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            },
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                ],
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        ],
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                "evidence": [
                    {
                        "id": "0050857",
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                ],
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            {
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                "url": "https://disease-ontology.org/term/DOID:0061117",
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                        "id": "0061117",
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                ],
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            },
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                        "id": "0110162",
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                ],
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            },
            {
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                        "id": "0110842",
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                    }
                ],
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            },
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                "evidence": [
                    {
                        "id": "2491",
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                ],
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                    {
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                ],
                "pmid": ""
            },
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            },
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                ],
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                ],
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            },
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                ],
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            },
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                ],
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            },
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                    }
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            }
        ],
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                ],
                "pmid": ""
            },
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                "name": "histone acetyltransferase complex",
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                    }
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            },
            {
                "name": "SAGA complex",
                "id": "GO:0000124",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000124",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "H3 histone acetyltransferase complex",
                "id": "GO:0070775",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070775",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome",
                "id": "GO:0005700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polytene chromosome puff",
                "id": "GO:0005703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005703",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATAC complex",
                "id": "GO:0140672",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140672",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006338",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription initiation-coupled chromatin remodeling",
                "id": "GO:0045815",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045815",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PHZ1",
                        "url": "https://www.uniprot.org/uniprotkb/M9PHZ1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9PI14-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 180,
        "chemical_mass": 21198.0,
        "gene_names": "Naa20A;CG14222;DmAAF48987;Dmel\\CG14222;Dmel_CG14222;NAA20;Naa20A;Naa20;dNAA20",
        "protein_name": "N-alpha-acetyltransferase 20",
        "disease": [
            {
                "disease_id": "DOID:0081233",
                "name": "autosomal recessive intellectual developmental disorder 73",
                "description": "An autosomal recessive intellectual developmental disorder that is characterized by global developmental delay with hypotonia and mildly delayed walking, impaired intellectual development with poor or absent speech, and mildly dysmorphic features and that has_material_basis_in homozygous mutation in the NAA20 gene on chromosome 20p11.",
                "url": "https://disease-ontology.org/term/DOID:0081233",
                "evidence": [
                    {
                        "id": "0081233",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081233"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NatB complex",
                "id": "GO:0031416",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031416",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of actin cytoskeleton organization",
                "id": "GO:0032956",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032956",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of neuron apoptotic process",
                "id": "GO:0043524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein-N-terminal amino-acid acetyltransferase activity",
                "id": "GO:0004596",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004596",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein N-terminal-methionine acetyltransferase activity",
                "id": "GO:0120518",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0120518",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI14",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI14"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9PI45-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 682,
        "chemical_mass": 71304.0,
        "gene_names": "mirr;CG10601;DH1;De1;De3;Dmel\\CG10601;Dmel_CG10601;Group F;IRO-C;Iro-C;IroC;Iro;MIRR;Mirr;Mrr;Sai;crep;cre;group F;iro-C;iro;l(3)69Ca;l(3)69Da;l(3)6D1;l(3)A5-3-42;mirr;mir;mrr",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "negative regulation of transcription by RNA polymerase II",
                "id": "GO:0000122",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000122",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron differentiation",
                "id": "GO:0030182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell development",
                "id": "GO:0048468",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048468",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory neuron axon guidance",
                "id": "GO:0097374",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097374",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of growth",
                "id": "GO:0045926",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045926",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "muscle cell fate commitment",
                "id": "GO:0042693",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042693",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "embryonic development via the syncytial blastoderm",
                "id": "GO:0001700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye morphogenesis",
                "id": "GO:0001745",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001745",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing vein specification",
                "id": "GO:0007474",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007474",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing morphogenesis",
                "id": "GO:0007476",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007476",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "equator specification",
                "id": "GO:0045317",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045317",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal appendage formation",
                "id": "GO:0046843",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046843",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein homodimerization activity",
                "id": "GO:0042803",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042803",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI45",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI45"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9PI57-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 834,
        "chemical_mass": 96325.0,
        "gene_names": "nan;CG5842;CT18317;DmNan;Dmel\\CG5842;Dmel_CG5842;Iav;NAN;Nan;OCR;TRPV;nan",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050534",
                "name": "congenital stationary night blindness",
                "description": "A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.",
                "url": "https://disease-ontology.org/term/DOID:0050534",
                "evidence": [
                    {
                        "id": "0050534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070355",
                "name": "overactive bladder syndrome",
                "description": "A bladder disease characterized by urinary urgency without urinary tract infection or obvious pathology, usually accompanied by urinary frequency and nocturia.",
                "url": "https://disease-ontology.org/term/DOID:0070355",
                "evidence": [
                    {
                        "id": "0070355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110182",
                "name": "Charcot-Marie-Tooth disease axonal type 2C",
                "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.",
                "url": "https://disease-ontology.org/term/DOID:0110182",
                "evidence": [
                    {
                        "id": "0110182",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110182"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110555",
                "name": "autosomal dominant nonsyndromic deafness 25",
                "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.",
                "url": "https://disease-ontology.org/term/DOID:0110555",
                "evidence": [
                    {
                        "id": "0110555",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110555"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111215",
                "name": "autosomal dominant distal hereditary motor neuronopathy 8",
                "description": "An autosomal dominant distal hereditary motor neuronopathy that is characterized by congenital, non-progressive, predominantly distal, lower limb muscle weakness and atrophy with variable severity that has_material_basis_in heterozygous mutation in the TRPV4 gene on 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111215",
                "evidence": [
                    {
                        "id": "0111215",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111215"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111514",
                "name": "metatropic dysplasia",
                "description": "A spondyloepimetaphyseal dysplasia characterized by short limbs with limitation and enlargement of joints, usually severe and progressive kyphoscoliosis, severe platyspondyly, and severe metaphyseal enlargement that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111514",
                "evidence": [
                    {
                        "id": "0111514",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111514"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111539",
                "name": "parastremmatic dwarfism",
                "description": "An osteochondrodysplasia characterized by severe dwarfism, kyphoscoliosis, stiffness of large joints and bowing and twisting of lower limbs that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111539",
                "evidence": [
                    {
                        "id": "0111539",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111539"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111552",
                "name": "scapuloperoneal spinal muscular atrophy",
                "description": "A motor neuron disease characterized by progressive scapuloperoneal atrophy and weakness, laryngeal palsy, congenital absence of muscles and in some cases developmental abnormalities of the bones that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111552",
                "evidence": [
                    {
                        "id": "0111552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111553",
                "name": "spondyloepiphyseal dysplasia Maroteaux type",
                "description": "An osteochondrodysplasia characterized by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, platyspondyly, severe brachydactyly, and pelvic abnormalities that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111553",
                "evidence": [
                    {
                        "id": "0111553",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111553"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111554",
                "name": "spondylometaphyseal dysplasia Kozlowski type",
                "description": "A spondylometaphyseal dysplasia characterized by vetebral platyspondyly and overfaced pedicles, scoliosis, and mild metaphyseal abnormalities in the pelvis that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.",
                "url": "https://disease-ontology.org/term/DOID:0111554",
                "evidence": [
                    {
                        "id": "0111554",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111554"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111711",
                "name": "focal nonepidermolytic palmoplantar keratoderma 2",
                "description": "A focal nonepidermolytic palmoplantar keratoderma that has_material_basis_in heterozygous mutation in the TRPV3 gene on chromosome 17p13.2.",
                "url": "https://disease-ontology.org/term/DOID:0111711",
                "evidence": [
                    {
                        "id": "0111711",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111711"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112013",
                "name": "autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques",
                "description": "A mutilating palmoplantar keratoderma with periorificial keratotic plaques that has_material_basis_in heterozygous mutation in the TRPV3 gene on chromosome 17p13.2.",
                "url": "https://disease-ontology.org/term/DOID:0112013",
                "evidence": [
                    {
                        "id": "0112013",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112013"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10024",
                "name": "migraine with aura",
                "description": "A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon.",
                "url": "https://disease-ontology.org/term/DOID:10024",
                "evidence": [
                    {
                        "id": "10024",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10024"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10159",
                "name": "osteonecrosis",
                "description": "An ischemic bone disease that results_in necrosis located_in bone.",
                "url": "https://disease-ontology.org/term/DOID:10159",
                "evidence": [
                    {
                        "id": "10159",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10159"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10591",
                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10808",
                "name": "gastric ulcer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10808",
                "evidence": [
                    {
                        "id": "10808",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10808"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11714",
                "name": "gestational diabetes",
                "description": "A diabetes mellitus that manifests during pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:11714",
                "evidence": [
                    {
                        "id": "11714",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11714"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13543",
                "name": "hyperparathyroidism",
                "description": "A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body.",
                "url": "https://disease-ontology.org/term/DOID:13543",
                "evidence": [
                    {
                        "id": "13543",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13543"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2548",
                "name": "reflex epilepsy",
                "description": "A variable age at onset electroclinical syndrome that is consistently induced by identifiable and objective-specific triggers, which may be an afferent stimulus or by the patient's own activity.",
                "url": "https://disease-ontology.org/term/DOID:2548",
                "evidence": [
                    {
                        "id": "2548",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2548"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2723",
                "name": "dermatitis",
                "description": "A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin.",
                "url": "https://disease-ontology.org/term/DOID:2723",
                "evidence": [
                    {
                        "id": "2723",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2723"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3310",
                "name": "atopic dermatitis",
                "description": "An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking.",
                "url": "https://disease-ontology.org/term/DOID:3310",
                "evidence": [
                    {
                        "id": "3310",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3310"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6364",
                "name": "migraine",
                "description": "A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing.",
                "url": "https://disease-ontology.org/term/DOID:6364",
                "evidence": [
                    {
                        "id": "6364",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6364"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:809",
                "name": "cocaine abuse",
                "description": "A substance abuse that involves the recurring use of cocaine despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:809",
                "evidence": [
                    {
                        "id": "809",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:809"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8881",
                "name": "rosacea",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8881",
                "evidence": [
                    {
                        "id": "8881",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8881"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9743",
                "name": "diabetic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9743",
                "evidence": [
                    {
                        "id": "9743",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9743"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:987",
                "name": "alopecia",
                "description": "A hypotrichosis that is characterized by a loss of hair from the head or body.",
                "url": "https://disease-ontology.org/term/DOID:987",
                "evidence": [
                    {
                        "id": "987",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:987"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "startle response",
                "id": "GO:0001964",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001964",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensory behavior",
                "id": "GO:0007638",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007638",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception of touch",
                "id": "GO:0050976",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050976",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception of sound",
                "id": "GO:0050910",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050910",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transport",
                "id": "GO:0006816",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006816",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic ion transmembrane transport",
                "id": "GO:0034220",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034220",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation transport",
                "id": "GO:0006812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adult walking behavior",
                "id": "GO:0007628",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007628",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to auditory stimulus",
                "id": "GO:0010996",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010996",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory perception of sound",
                "id": "GO:0007605",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007605",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion transmembrane transport",
                "id": "GO:0070588",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070588",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "detection of mechanical stimulus involved in sensory perception",
                "id": "GO:0050974",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050974",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuromuscular process controlling posture",
                "id": "GO:0050884",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050884",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion import across plasma membrane",
                "id": "GO:0098703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098703",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to humidity",
                "id": "GO:0009270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative gravitaxis",
                "id": "GO:0048060",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048060",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mechanosensory behavior",
                "id": "GO:1905790",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905790",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cation channel complex",
                "id": "GO:0034703",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034703",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium channel complex",
                "id": "GO:0034704",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034704",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "monoatomic ion channel activity",
                "id": "GO:0005216",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005216",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium channel activity",
                "id": "GO:0005262",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005262",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic cation channel activity",
                "id": "GO:0005261",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005261",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensitive monoatomic ion channel activity",
                "id": "GO:0008381",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008381",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mechanosensitive monoatomic cation channel activity",
                "id": "GO:0140135",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140135",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PI57",
                        "url": "https://www.uniprot.org/uniprotkb/M9PI57"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "M9PIC9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1960,
        "chemical_mass": 223190.0,
        "gene_names": "Spc105R;CG11451;DmSpc105;Dmel\\CG11451;Dmel_CG11451;KNL1;Spc105-R;Spc105R;Spc105r;Spc105;dmKNL-1;dmSpc105R;spc105R;spc105r",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "kinetochore assembly",
                "id": "GO:0051382",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051382",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "attachment of spindle microtubules to kinetochore",
                "id": "GO:0008608",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008608",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "outer kinetochore",
                "id": "GO:0000940",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000940",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIC9",
                        "url": "https://www.uniprot.org/uniprotkb/M9PIC9"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "M9PIC9-1",
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                "end_pos": "1349",
                "site_lbl": "Thr1349",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1349,
                        "start_aa": "Thr",
                        "end_pos": 1349,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1349",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "M9PIM3-1",
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9PIM3",
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                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 118749.0,
        "gene_names": "Dmel\\CG43968;CG43968;Dmel\\CG43968;Dmel_CG43968;lincRNA.665",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "O16043-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 18823.0,
        "gene_names": "Df31;BEST:LD04967;CG2207;DF 31;DF31;Df31;Dmel\\CG2207;Dmel_CG2207;LD04967;anon-EST:Liang-1.46;anon-EST:Posey126;anon-EST:fe1A4;anon-WO0153538.53;anon1A4;clone 1.46;l(2)k05815",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin organization",
                "id": "GO:0006325",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006325",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleosome assembly",
                "id": "GO:0006334",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006334",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "histone binding",
                "id": "GO:0042393",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042393",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O16043",
                        "url": "https://www.uniprot.org/uniprotkb/O16043"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "O17452-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
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                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 25492.0,
        "gene_names": "PeriA;CG17058;CG31559;Dmel\\CG17058;Dmel_CG17058;PeriA;Peritrophin-A;obst-D",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
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                    {
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                        "id": "O17452",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "external encapsulating structure",
                "id": "GO:0030312",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030312",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
                        "url": "https://www.uniprot.org/uniprotkb/O17452"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "structural constituent of chitin-based cuticle",
                "id": "GO:0005214",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005214",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O17452",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "O62526-1",
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                        "database": "UniProtKB",
                        "id": "O62526",
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                    }
                ],
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            }
        ],
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        "gene_names": "Ant2;ANT2;Ant2;CG1683;Dmel\\CG1683;Dmel_CG1683;FBgn0025111;l(1)G0126;l(1)G0247;l(1)G0386",
        "protein_name": "ADP/ATP translocase",
        "disease": [
            {
                "disease_id": "DOID:0080130",
                "name": "mitochondrial DNA depletion syndrome 12a",
                "description": "A mitochondrial DNA depletion syndrome that is characterized by severe hypotonia due to mitochondrial dysfunction apparent at birth and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 25 member 4 gene on chromosome 4q35.",
                "url": "https://disease-ontology.org/term/DOID:0080130",
                "evidence": [
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0080335",
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                "description": "A mitochondrial DNA depletion syndrome that is characterized by childhood onset of slowly progressive hypertrophic cardiomyopathy and generalized skeletal myopathy resulting in exercise intolerance, muscle weakness, and atrophy, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the the solute carrier family 25 member 4 on chromosome 4q35.",
                "url": "https://disease-ontology.org/term/DOID:0080335",
                "evidence": [
                    {
                        "id": "0080335",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0110429",
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                "description": "A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 2q14-q22.",
                "url": "https://disease-ontology.org/term/DOID:0110429",
                "evidence": [
                    {
                        "id": "0110429",
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                    }
                ],
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            },
            {
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                "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2",
                "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the SLC25A4 gene on chromosome 4q35.1.",
                "url": "https://disease-ontology.org/term/DOID:0111517",
                "evidence": [
                    {
                        "id": "0111517",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0111517"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
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                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
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                ],
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            },
            {
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                    }
                ],
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            },
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                    }
                ],
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            },
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                    }
                ],
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                    }
                ],
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            },
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                    }
                ],
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            },
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                ],
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            }
        ],
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                ],
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            },
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        ],
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                    }
                ],
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        ],
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        ],
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    },
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        "gene_names": "EG:100G10.1;CG2685;Dmel\\CG2685;Dmel_CG2685;EG:100G10.1",
        "protein_name": "Wbp11/ELF5/Saf1 N-terminal domain-containing protein",
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            {
                "name": "RNA binding",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
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            },
            {
                "name": "protein phosphatase regulator activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019888",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "RNA splicing",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008380",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA splicing, via spliceosome",
                "id": "GO:0000398",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000398",
                "evidence": [
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "catalytic step 2 spliceosome",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "precatalytic spliceosome",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
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            }
        ],
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            {
                "uniprot_canonical_ac": "O76861-1",
                "start_pos": "361",
                "end_pos": "361",
                "site_lbl": "Thr361",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 361,
                        "start_aa": "Thr",
                        "end_pos": 361,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr361",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "O76861-1",
                "start_pos": "368",
                "end_pos": "368",
                "site_lbl": "Thr368",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 368,
                        "start_aa": "Thr",
                        "end_pos": 368,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr368",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "O96660-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 486,
        "chemical_mass": 53677.0,
        "gene_names": "Smox;3;CG2262;DSMAD2;DSmad2;Dmel\\CG2262;SMAD2;SMOX;Sad;Smad2/3;Smad2;Smad;SmoX;Smox;dSMAD2;dSmad2;dSmad;dsmad2;l(1)G0348;sad;smad2;smox;ted;tmp",
        "protein_name": "SMAD family member 2",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060071",
                "name": "pre-malignant neoplasm",
                "description": "A disease of cellular proliferation that results in abnormal growths in the body, which do not invade or destroy the surrounding tissue but, given enough time, will transform into a cancer.",
                "url": "https://disease-ontology.org/term/DOID:0060071",
                "evidence": [
                    {
                        "id": "0060071",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060071"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060964",
                "name": "Loeys-Dietz syndrome 6",
                "description": "A Loeys-Dietz syndrome characterized by aortic/arterial aneurysm and dissection in association with connective tissue findings that has_material_basis_in heterozygous mutation in the SMAD2 gene (601366) on chromosome 18q21.",
                "url": "https://disease-ontology.org/term/DOID:0060964",
                "evidence": [
                    {
                        "id": "0060964",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060964"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070237",
                "name": "Loeys-Dietz syndrome 3",
                "description": "A Loeys-Dietz syndrome that has_material_basis_in heterozygous mutation in the SMAD3 gene on chromosome 15q.",
                "url": "https://disease-ontology.org/term/DOID:0070237",
                "evidence": [
                    {
                        "id": "0070237",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070237"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10892",
                "name": "hypospadias",
                "description": "A physical disorder characterized by an abnormally placed urethral opening on the underside of the penis or on the perineum.",
                "url": "https://disease-ontology.org/term/DOID:10892",
                "evidence": [
                    {
                        "id": "10892",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10892"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12935",
                "name": "alcoholic cardiomyopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12935",
                "evidence": [
                    {
                        "id": "12935",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12935"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1380",
                "name": "endometrial cancer",
                "description": "A uterine cancer that is located_in tissues lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:1380",
                "evidence": [
                    {
                        "id": "1380",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1380"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3498",
                "name": "pancreatic ductal adenocarcinoma",
                "description": "A pancreatic adenocarcinoma that derives_from pancreatic duct cells.",
                "url": "https://disease-ontology.org/term/DOID:3498",
                "evidence": [
                    {
                        "id": "3498",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3498"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3744",
                "name": "cervical squamous cell carcinoma",
                "description": "A cervix carcinoma that has_material_basis_in squamous cells of the cervix.",
                "url": "https://disease-ontology.org/term/DOID:3744",
                "evidence": [
                    {
                        "id": "3744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3883",
                "name": "Lynch syndrome",
                "description": "A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.",
                "url": "https://disease-ontology.org/term/DOID:3883",
                "evidence": [
                    {
                        "id": "3883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3883"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4001",
                "name": "ovarian carcinoma",
                "description": "An ovarian cancer that has_material_basis_in epithelial tissue and is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:4001",
                "evidence": [
                    {
                        "id": "4001",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4001"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4362",
                "name": "cervical cancer",
                "description": "A female reproductive organ cancer that is located_in the cervix.",
                "url": "https://disease-ontology.org/term/DOID:4362",
                "evidence": [
                    {
                        "id": "4362",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4362"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8398",
                "name": "osteoarthritis",
                "description": "An arthritis that has_material_basis_in worn out cartilage located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:8398",
                "evidence": [
                    {
                        "id": "8398",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8398"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9975",
                "name": "cocaine dependence",
                "description": "A drug dependence that is a psychological dependency on the regular use of cocaine.",
                "url": "https://disease-ontology.org/term/DOID:9975",
                "evidence": [
                    {
                        "id": "9975",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9975"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "positive regulation of glycogen catabolic process",
                "id": "GO:0045819",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045819",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by RNA polymerase II",
                "id": "GO:0045944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of synapse structure or activity",
                "id": "GO:0050803",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050803",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to glucose stimulus",
                "id": "GO:0071333",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071333",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of autophagy",
                "id": "GO:0010507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SMAD protein signal transduction",
                "id": "GO:0060395",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060395",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "activin receptor signaling pathway",
                "id": "GO:0032924",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032924",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dendrite morphogenesis",
                "id": "GO:0048813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron development",
                "id": "GO:0048666",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048666",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of neuroblast proliferation",
                "id": "GO:0002052",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002052",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "anatomical structure morphogenesis",
                "id": "GO:0009653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell proliferation involved in imaginal disc-derived wing morphogenesis",
                "id": "GO:0090256",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090256",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc growth",
                "id": "GO:0007446",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007446",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing morphogenesis",
                "id": "GO:0007476",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007476",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mushroom body development",
                "id": "GO:0016319",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016319",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of imaginal disc-derived wing size",
                "id": "GO:0044719",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044719",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "R8 cell fate specification",
                "id": "GO:0045464",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045464",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
                        "url": "https://www.uniprot.org/uniprotkb/O96660"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of imaginal disc growth",
                "id": "GO:0045572",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045572",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O96660",
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                "name": "extracellular matrix organization",
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                "name": "synaptic target recognition",
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            {
                "name": "zinc ion binding",
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        ],
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                "name": "regulation of transcription by RNA polymerase II",
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                "name": "mRNA regulatory element binding translation repressor activity",
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                "name": "proton-transporting V-type ATPase complex",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of cellular pH",
                "id": "GO:0030641",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030641",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic vesicle lumen acidification",
                "id": "GO:0097401",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097401",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ATPase regulator activity",
                "id": "GO:0060590",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060590",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHY8",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHY8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VDI5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 281,
        "chemical_mass": 32536.0,
        "gene_names": "Dm_3R:88623;Dmel\\CG17271;CG17271;Dm_3R:88623;Dmel\\CG17271;Dmel_CG17271",
        "protein_name": "EF-hand domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum",
                "id": "GO:0005783",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005783",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "calcium ion binding",
                "id": "GO:0005509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VDI5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDI5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q0KIE7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1549,
        "chemical_mass": 170168.0,
        "gene_names": "Ank;ANK;Ank;CG1651;CG32008;DAnk1;Dank1;Dmel\\CG1651;Dmel_CG1651;ank;dank1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050668",
                "name": "alcohol-related birth defects",
                "description": "A fetal alcohol spectrum disorder that results in damage to organs, bones, or muscles due to prenatal alcohol exposure.",
                "url": "https://disease-ontology.org/term/DOID:0050668",
                "evidence": [
                    {
                        "id": "0050668",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050668"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050824",
                "name": "sinoatrial node disease",
                "description": "A heart conduction disease that is characterized by dysfunction of the impulse-generating (pacemaker) tissue located in the right atrium of the heart which generates normal sinus rhythm.",
                "url": "https://disease-ontology.org/term/DOID:0050824",
                "evidence": [
                    {
                        "id": "0050824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060224",
                "name": "atrial fibrillation",
                "description": "A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.",
                "url": "https://disease-ontology.org/term/DOID:0060224",
                "evidence": [
                    {
                        "id": "0060224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081202",
                "name": "autosomal recessive intellectual developmental disorder 37",
                "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ANK3 gene on chromosome 10q21.",
                "url": "https://disease-ontology.org/term/DOID:0081202",
                "evidence": [
                    {
                        "id": "0081202",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081202"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110916",
                "name": "hereditary spherocytosis type 1",
                "description": "A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the ANK1 gene on chromosome 8p11.21.",
                "url": "https://disease-ontology.org/term/DOID:0110916",
                "evidence": [
                    {
                        "id": "0110916",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110916"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111700",
                "name": "ankyrin-B-related cardiac arrhythmia",
                "description": "A heart disease characterized by a broad spectrum of cardiac arrhythmias including; bradycardia, sinus arrhythmia, delayed conduction/conduction block, idiopathic ventricular fibrillation, and catecholaminergic polymorphic ventricular tachycardia that has_material_basis_in heterozygous mutation in the ANK2 gene on chromosome 4q25-q26.",
                "url": "https://disease-ontology.org/term/DOID:0111700",
                "evidence": [
                    {
                        "id": "0111700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111700"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12365",
                "name": "malaria",
                "description": "A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle.",
                "url": "https://disease-ontology.org/term/DOID:12365",
                "evidence": [
                    {
                        "id": "12365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12849",
                "name": "autistic disorder",
                "description": "An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years.",
                "url": "https://disease-ontology.org/term/DOID:12849",
                "evidence": [
                    {
                        "id": "12849",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12849"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12971",
                "name": "hereditary spherocytosis",
                "description": "A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape.",
                "url": "https://disease-ontology.org/term/DOID:12971",
                "evidence": [
                    {
                        "id": "12971",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12971"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13884",
                "name": "sick sinus syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13884",
                "evidence": [
                    {
                        "id": "13884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13884"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1824",
                "name": "status epilepticus",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1824",
                "evidence": [
                    {
                        "id": "1824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2055",
                "name": "post-traumatic stress disorder",
                "description": "An anxiety disorder which results from a traumatic experience that results in psychological trauma.",
                "url": "https://disease-ontology.org/term/DOID:2055",
                "evidence": [
                    {
                        "id": "2055",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2055"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
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                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:2843",
                "name": "long QT syndrome",
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                "url": "https://disease-ontology.org/term/DOID:2843",
                "evidence": [
                    {
                        "id": "2843",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2843"
                    }
                ],
                "weight": 0.0
            },
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                "name": "bipolar disorder",
                "description": "A mood disorder that involves alternating periods of mania and depression.",
                "url": "https://disease-ontology.org/term/DOID:3312",
                "evidence": [
                    {
                        "id": "3312",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3312"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.",
                "url": "https://disease-ontology.org/term/DOID:5419",
                "evidence": [
                    {
                        "id": "5419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5419"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection",
                "id": "GO:0043005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "spectrosome",
                "id": "GO:0045170",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045170",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to plasma membrane",
                "id": "GO:0072659",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072659",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter binding",
                "id": "GO:0044325",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044325",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "spectrin binding",
                "id": "GO:0030507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoskeletal anchor activity",
                "id": "GO:0008093",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008093",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KIE7",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KIE7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q0KIE7-1",
                "start_pos": "1538",
                "end_pos": "1538",
                "site_lbl": "Thr1538",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1538,
                        "start_aa": "Thr",
                        "end_pos": 1538,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1538",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q2MGM0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2MGM0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2MGM0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 606,
        "chemical_mass": 70985.0,
        "gene_names": "Ir62a;62a;CG12090;CG33971;DmelIR62a;Dmel\\CG33971;Dmel_CG33971;IR62a;Ir62a",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "detection of chemical stimulus",
                "id": "GO:0009593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2MGM0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2MGM0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2MGM0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2MGM0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2MGM0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2MGM0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ligand-gated monoatomic ion channel activity",
                "id": "GO:0015276",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015276",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2MGM0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2MGM0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q2PDQ0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q2PDQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q2PDQ0"
                    }
                ],
                "common_name": "Fruit fly",
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                ],
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                "name": "advanced sleep phase syndrome 4",
                "description": "An advanced sleep phase syndrome that has_material_basis_in heterozygous mutation in the TIMELESS gene on chromosome 12q13.",
                "url": "https://disease-ontology.org/term/DOID:0061006",
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                    {
                        "id": "0061006",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061006"
                    }
                ],
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            },
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                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
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                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "DNA replication checkpoint signaling",
                "id": "GO:0000076",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000076",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA repair",
                "id": "GO:0006281",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006281",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "entrainment of circadian clock",
                "id": "GO:0009649",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009649",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA damage checkpoint signaling",
                "id": "GO:0000077",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000077",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "replication fork arrest",
                "id": "GO:0043111",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043111",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "replication fork protection complex",
                "id": "GO:0031298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INH7",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INH7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
    {
        "uniprot_canonical_ac": "Q8INK3-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INK3"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 17137.0,
        "gene_names": "fabp;BcDNA:RH06221;BcDNA:RH46282;BcDNA:RH49003;BcDNA:SD12036;CG31305-PI;CG31305;CG6783;CT21061;Dmel\\CG6783;Dmel_CG6783;FABP;Fabp;anon-EST:Posey234;anon-WO0140519.12;dFABP;dFabp;fabp",
        "protein_name": "Fatty acid-binding protein, muscle",
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                "disease_id": "DOID:0111560",
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                "url": "https://disease-ontology.org/term/DOID:0111560",
                "evidence": [
                    {
                        "id": "0111560",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111560"
                    }
                ],
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            },
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                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
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                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
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                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
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            },
            {
                "disease_id": "DOID:14250",
                "name": "Down syndrome",
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                "url": "https://disease-ontology.org/term/DOID:14250",
                "evidence": [
                    {
                        "id": "14250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14250"
                    }
                ],
                "weight": 0.0
            },
            {
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                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1875",
                "name": "impotence",
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                "url": "https://disease-ontology.org/term/DOID:1875",
                "evidence": [
                    {
                        "id": "1875",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1875"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3068",
                "name": "glioblastoma",
                "description": "A malignant astrocytoma characterized by the presence of small areas of necrotizing tissue that is surrounded by anaplastic cells as well as the presence of hyperplastic blood vessels, and that has_material_basis_in abnormally proliferating cells derives_from multiple cell types including astrocytes and oligondroctyes.",
                "url": "https://disease-ontology.org/term/DOID:3068",
                "evidence": [
                    {
                        "id": "3068",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3068"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
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                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
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            },
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                "name": "muscular atrophy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:767",
                "evidence": [
                    {
                        "id": "767",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:767"
                    }
                ],
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            },
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                "name": "psoriasis",
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                "url": "https://disease-ontology.org/term/DOID:8893",
                "evidence": [
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                        "id": "8893",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8893"
                    }
                ],
                "weight": 0.0
            },
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                "evidence": [
                    {
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
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                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
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                    }
                ],
                "weight": 0.0
            }
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            {
                "name": "fatty acid binding",
                "id": "GO:0005504",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005504",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q8INK3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
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                    }
                ],
                "pmid": ""
            },
            {
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                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INK3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "long-term memory",
                "id": "GO:0007616",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007616",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "fatty acid transport",
                "id": "GO:0015908",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015908",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
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                    }
                ],
                "pmid": ""
            },
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                "name": "chitin-based cuticle development",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INK3",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "Q8INM2-1",
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            {
                "name": "Drosophila melanogaster",
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                        "id": "Q8INM2",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
        "length": 249,
        "chemical_mass": 27169.0,
        "gene_names": "Dmel\\CG31406;BcDNA:AT13367;CG31406;Dmel\\CG31406;Dmel_CG31406",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "notum morphogenesis",
                "id": "GO:0048802",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048802",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INM2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INM2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8INX1-1",
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                "name": "Drosophila melanogaster",
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                        "id": "Q8INX1",
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                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 182,
        "chemical_mass": 21029.0,
        "gene_names": "Dmel\\CG31800;CG31800;Dmel\\CG31800;Dmel_CG31800",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8INX4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INX4",
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                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 498,
        "chemical_mass": 58339.0,
        "gene_names": "Mst36Fa;CG15165;CG31801;Dmel\\CG31801;Dmel_CG31801;Mst36Fa;mst36Fa",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "spermatogenesis",
                "id": "GO:0007283",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007283",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INX4",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INX4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8INX6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INX6",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INX6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 117,
        "chemical_mass": 12580.0,
        "gene_names": "Dmel\\CG31789;CG31789;Dmel\\CG31789;Dmel_CG31789",
        "protein_name": "Salivary secreted peptide",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8INY2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INY2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INY2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 380,
        "chemical_mass": 44246.0,
        "gene_names": "Grl36b;CG31785;Dmel\\CG31785;Dmel_CG31785;Grl36b",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INY2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INY2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INY2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INY2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ligand-gated channel activity",
                "id": "GO:0022834",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022834",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8INY2",
                        "url": "https://www.uniprot.org/uniprotkb/Q8INY2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q8IP91-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP91"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 564,
        "chemical_mass": 64164.0,
        "gene_names": "d3635;3635;BcDNA:AT13596;BcDNA:LD05405;CG31759;Dmel\\CG31759;Dmel_CG31759;d3635;ms(2)01284",
        "protein_name": "2',5'-phosphodiesterase 12",
        "disease": [],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP91"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP91"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mRNA processing",
                "id": "GO:0006397",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006397",
                "evidence": [
                    {
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                        "id": "Q8IP91",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP91"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial RNA 3'-end processing",
                "id": "GO:0000965",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000965",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
                        "url": "https://www.uniprot.org/uniprotkb/Q8IP91"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000288",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial mRNA catabolic process",
                "id": "GO:0000958",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8IP91",
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                    }
                ],
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            }
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "3'-5'-RNA exonuclease activity",
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                    {
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                    }
                ],
                "pmid": ""
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            {
                "name": "poly(A)-specific ribonuclease activity",
                "id": "GO:0004535",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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        ],
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            {
                "name": "transcription coactivator activity",
                "id": "GO:0003713",
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                    {
                        "database": "UniProtKB",
                        "id": "Q8IP99",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "SAGA complex",
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                ],
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        ],
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            {
                "name": "DNA-templated transcription",
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                ],
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            {
                "name": "regulation of transcription by RNA polymerase II",
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                    {
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                    }
                ],
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            },
            {
                "name": "positive regulation of DNA-templated transcription",
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                    {
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                    }
                ],
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        ],
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    {
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                ],
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        ],
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    {
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                ],
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        ],
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            {
                "name": "nucleus",
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                ],
                "pmid": ""
            },
            {
                "name": "MLL1 complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071339",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "NURF complex",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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        ],
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                        "id": "3413",
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                ],
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        ],
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            {
                "name": "extracellular region",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosome",
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                    {
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                ],
                "pmid": ""
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        ],
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            {
                "name": "metal ion binding",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "carbohydrate binding",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "alpha-mannosidase activity",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mannosyl-oligosaccharide 1,2-alpha-mannosidase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004571",
                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
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        ],
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            {
                "name": "mannose metabolic process",
                "id": "GO:0006013",
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                    {
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
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                ],
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            },
            {
                "name": "chitin-based extracellular matrix",
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                ],
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        ],
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                "name": "structural constituent of chitin-based larval cuticle",
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                ],
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        ],
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            {
                "name": "chitin-based cuticle development",
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                ],
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        ],
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    {
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                ],
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        ],
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                "disease_id": "DOID:0080261",
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                ],
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            },
            {
                "disease_id": "DOID:0110463",
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                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
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                ],
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        ],
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                "name": "olfactory behavior",
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            {
                "name": "memory",
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                "name": "regulation of synapse structure or activity",
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                ],
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                "name": "Rho protein signal transduction",
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            {
                "name": "regulation of Rho protein signal transduction",
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                "name": "cytoplasm",
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                "name": "plasma membrane",
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                "name": "ubiquitin protein ligase binding",
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        ],
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                "name": "mRNA binding",
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                ],
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        ],
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    {
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                ],
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                "name": "nucleus",
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                ],
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        ],
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                "name": "ribonuclease inhibitor activity",
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        ],
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                ],
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                "name": "negative regulation of transcription by RNA polymerase II",
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                ],
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            {
                "name": "dendrite morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V3X8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V3X8"
                    }
                ],
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            }
        ],
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                "name": "nucleus",
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                ],
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            {
                "name": "zinc ion binding",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V3X8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V3X8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II transcription regulatory region sequence-specific DNA binding",
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                    {
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                ],
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            },
            {
                "name": "DNA-binding transcription repressor activity, RNA polymerase II-specific",
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                "name": "extracellular region",
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                "name": "melanin biosynthetic process from tyrosine",
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                "name": "dopaminechrome tautomerase activity",
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                ],
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                "name": "pyrimidine-specific mismatch base pair DNA N-glycosylase activity",
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                ],
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                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
                "id": "GO:0005730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005730",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription initiation at RNA polymerase I promoter",
                "id": "GO:0006361",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006361",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolar large rRNA transcription by RNA polymerase I",
                "id": "GO:0042790",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042790",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "female germ-line stem cell population maintenance",
                "id": "GO:0036099",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036099",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "RNA polymerase I general transcription initiation factor activity",
                "id": "GO:0001181",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001181",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase I core binding",
                "id": "GO:0001042",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001042",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9M6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9M6"
                    }
                ],
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            }
        ],
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            {
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                    {
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                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
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                        },
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                        "relation": "attached",
                        "comment": "",
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                            }
                        ]
                    }
                ]
            }
        ],
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    {
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            {
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                        "id": "Q9V9T1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9T1"
                    }
                ],
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            }
        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9T1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9T1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Cul4-RING E3 ubiquitin ligase complex",
                "id": "GO:0080008",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0080008",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9T1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9T1"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "negative regulation of fatty acid biosynthetic process",
                "id": "GO:0045717",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045717",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9T1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9T1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9V9U1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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            {
                "disease_id": "DOID:0050328",
                "name": "congenital hypothyroidism",
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                    {
                        "id": "0050328",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0112185",
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                "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in SLC5A5 on chromosome 19p13.11.",
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                "evidence": [
                    {
                        "id": "0112185",
                        "database": "AGR",
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                ],
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        ],
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            {
                "name": "D-glucose:sodium symporter activity",
                "id": "GO:0005412",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005412",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "symporter activity",
                "id": "GO:0015293",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015293",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "glucose homeostasis",
                "id": "GO:0042593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transport",
                "id": "GO:0006814",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006814",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "D-glucose import across plasma membrane",
                "id": "GO:0098708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098708",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9U1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9U1"
                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                        "id": "Q9V9W4",
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                ],
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        "protein_name": "HotDog ACOT-type domain-containing protein",
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            {
                "name": "acetyl-CoA hydrolase activity",
                "id": "GO:0003986",
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                        "database": "UniProtKB",
                        "id": "Q9V9W4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W4"
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                "pmid": ""
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            {
                "name": "fatty acyl-CoA hydrolase activity",
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                    {
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                        "id": "Q9V9W4",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "mitochondrion",
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                    {
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                        "id": "Q9V9W4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W4"
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "acyl-CoA metabolic process",
                "id": "GO:0006637",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006637",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9W4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9W4"
                    }
                ],
                "pmid": ""
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        ],
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    {
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            {
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                ],
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        ],
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        "disease": [
            {
                "disease_id": "DOID:0070239",
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                "description": "A primary coenzyme Q10 deficiency that has_material_basis_in an autosomal recessive mutation of the PDSS1 gene on chromosome 10p12.1.",
                "url": "https://disease-ontology.org/term/DOID:0070239",
                "evidence": [
                    {
                        "id": "0070239",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070239"
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                ],
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        ],
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            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial inner membrane",
                "id": "GO:0005743",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005743",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heterotetrameric polyprenyl diphosphate synthase complex",
                "id": "GO:0032478",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032478",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "polyprenyl diphosphate synthase complex",
                "id": "GO:0032476",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032476",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
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        ],
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            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
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                ],
                "pmid": ""
            },
            {
                "name": "prenyltransferase activity",
                "id": "GO:0004659",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004659",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "all-trans-decaprenyl-diphosphate synthase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097269",
                "evidence": [
                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
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                ],
                "pmid": ""
            },
            {
                "name": "prenyl diphosphate synthase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ubiquinone biosynthetic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006744",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
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                ],
                "pmid": ""
            },
            {
                "name": "isoprenoid biosynthetic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008299",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9V9Z3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
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                ],
                "pmid": ""
            },
            {
                "name": "pheromone biosynthetic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042811",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9V9Z3"
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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        "protein_name": "",
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    {
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                        "id": "Q9VA09",
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                ],
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        ],
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        "protein_name": "Guanylate cyclase soluble subunit beta-1",
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                "disease_id": "DOID:0060001",
                "name": "withdrawal disorder",
                "description": "A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0060001",
                "evidence": [
                    {
                        "id": "0060001",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060001"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
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                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "guanylate cyclase activity",
                "id": "GO:0004383",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004383",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "GTP binding",
                "id": "GO:0005525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heme binding",
                "id": "GO:0020037",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0020037",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cGMP biosynthetic process",
                "id": "GO:0006182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to oxygen levels",
                "id": "GO:0070482",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070482",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "guanylate cyclase complex, soluble",
                "id": "GO:0008074",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008074",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA09",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA09"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VA09-1",
                "start_pos": "750",
                "end_pos": "750",
                "site_lbl": "Thr750",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 750,
                        "start_aa": "Thr",
                        "end_pos": 750,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr750",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VA17-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 529,
        "chemical_mass": 57069.0,
        "gene_names": "Sox100B;CG12098;CG15552;CG18674;CT6009;Dmel\\CG15552;Dmel_CG15552;SOX100B;SOXE;Sox100B;Sox100;Sox9;SoxB;dSox9",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050463",
                "name": "campomelic dysplasia",
                "description": "An osteochondrodysplasia that has_material_basis_in heterozygous mutation in the SOX9 gene on chromosome 17q24 and that is characterized by congenital shortness and bowing of long tubular bones, especially in the lower extremities, as well as by hypoplastic scapulae, narrow iliac wings, and nonmineralized thoracic pedicles.",
                "url": "https://disease-ontology.org/term/DOID:0050463",
                "evidence": [
                    {
                        "id": "0050463",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050463"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090111",
                "name": "PCWH syndrome",
                "description": "A syndrome that is characterized by the association of the features of Waardenburg-Shah syndrome (sensorineural hearing loss, pigmentary abnormalities and Hirschsprung disease; see this term) with neurological features, including: neonatal hypotonia, intellectual deficit (of variable severity), nystagmus, progressive spasticity, ataxia and epilepsy, and has_material_basis_in heterozygous mutation in the SRY-box 10 (SOX10) gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0090111",
                "evidence": [
                    {
                        "id": "0090111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110955",
                "name": "Waardenburg syndrome type 4C",
                "description": "A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous mutation in the SOX10 gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0110955",
                "evidence": [
                    {
                        "id": "0110955",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110955"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110956",
                "name": "Waardenburg syndrome type 2E",
                "description": "A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in heterozygous mutations in the SOX10 gene on chromosome 22q13.",
                "url": "https://disease-ontology.org/term/DOID:0110956",
                "evidence": [
                    {
                        "id": "0110956",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110956"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111763",
                "name": "46,XX sex reversal 2",
                "description": "A 46,XX sex reversal that has_material_basis_in heterozygous duplication or triplication of a 68-kb regulatory region -584 to -516 kb upstream of the SOX9 gene on chromosome 17q24.",
                "url": "https://disease-ontology.org/term/DOID:0111763",
                "evidence": [
                    {
                        "id": "0111763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111775",
                "name": "46,XY sex reversal 10",
                "description": "A 46 XY sex reversal characterized by an XY karyotype, phenotypically female genitalia and failure to develop secondary sexual characteristics at puberty including menstruation that has_material_basis_in heterozygous deletion of a region upstream of the SOX9 gene on chromosome 17q24.",
                "url": "https://disease-ontology.org/term/DOID:0111775",
                "evidence": [
                    {
                        "id": "0111775",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111775"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10487",
                "name": "Hirschsprung's disease",
                "description": "A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel.",
                "url": "https://disease-ontology.org/term/DOID:10487",
                "evidence": [
                    {
                        "id": "10487",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10487"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3614",
                "name": "Kallmann syndrome",
                "description": "A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia).",
                "url": "https://disease-ontology.org/term/DOID:3614",
                "evidence": [
                    {
                        "id": "3614",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3614"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3905",
                "name": "lung carcinoma",
                "description": "A lung cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells and is located_in the lungs and has_symptom cough and has_symptom chest discomfort or pain and has_symptom weight loss and has_symptom hemoptysis.",
                "url": "https://disease-ontology.org/term/DOID:3905",
                "evidence": [
                    {
                        "id": "3905",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3905"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9258",
                "name": "Waardenburg syndrome",
                "description": "A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes.",
                "url": "https://disease-ontology.org/term/DOID:9258",
                "evidence": [
                    {
                        "id": "9258",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9258"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "male gonad development",
                "id": "GO:0008584",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008584",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA17",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA17"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VA23-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA23",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA23"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 814,
        "chemical_mass": 94753.0,
        "gene_names": "Dmel\\CG15548;CG15548;Dmel\\CG15548;Dmel_CG15548",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VA48-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 649,
        "chemical_mass": 72745.0,
        "gene_names": "Spn100A;CG1342;Dmel\\CG1342;Dmel_CG1342;Spn100A;Spn100",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of immune response",
                "id": "GO:0050776",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050776",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA48"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VA79-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 486,
        "chemical_mass": 53744.0,
        "gene_names": "UIP5;CG2218;Dmel\\CG2218;Dmel_CG2218;UIP5",
        "protein_name": "U-box domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin protein ligase binding",
                "id": "GO:0031625",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031625",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin-ubiquitin ligase activity",
                "id": "GO:0034450",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034450",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin-protein transferase activity",
                "id": "GO:0004842",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004842",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein ubiquitination",
                "id": "GO:0016567",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016567",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein polyubiquitination",
                "id": "GO:0000209",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000209",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VA79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VA79"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VAD4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAD4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAD4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 306,
        "chemical_mass": 34395.0,
        "gene_names": "eIF2Balpha;CG7883;DeIF2Balpha;Dmel\\CG7883;Dmel_CG7883;Eif2b;eIF2B-alpha;eIF2Balpha",
        "protein_name": "Translation initiation factor eIF2B subunit alpha",
        "disease": [
            {
                "disease_id": "DOID:0060868",
                "name": "leukoencephalopathy with vanishing white matter",
                "description": "A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood.",
                "url": "https://disease-ontology.org/term/DOID:0060868",
                "evidence": [
                    {
                        "id": "0060868",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060868"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070374",
                "name": "leukoencephalopathy with vanishing white matter 1",
                "description": "A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B1 gene on chromosome 12q24.",
                "url": "https://disease-ontology.org/term/DOID:0070374",
                "evidence": [
                    {
                        "id": "0070374",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070374"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
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        ],
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            {
                "name": "translation initiation factor activity",
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    {
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                ],
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                "name": "metal ion binding",
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                ],
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        ],
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                ],
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        ],
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                "start_pos": "1995",
                "end_pos": "1995",
                "site_lbl": "Thr1995",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1995,
                        "start_aa": "Thr",
                        "end_pos": 1995,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1995",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VAY0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VAY0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAY0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 717,
        "chemical_mass": 82103.0,
        "gene_names": "Nep7;CG5527;Dmel\\CG5527;Dmel_CG5527;Nep7",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050646",
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                "description": "A muscle tissue disease characterized by congenital joint contractures of hand and feet.",
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                "evidence": [
                    {
                        "id": "0050646",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050646"
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                ],
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                "disease_id": "DOID:10652",
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                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
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                ],
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            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
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                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
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                ],
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                "disease_id": "DOID:13250",
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                "url": "https://disease-ontology.org/term/DOID:13250",
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                    {
                        "id": "13250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13250"
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                ],
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                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
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                    {
                        "id": "684",
                        "database": "AGR",
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                ],
                "weight": 0.0
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        ],
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            {
                "name": "metalloendopeptidase activity",
                "id": "GO:0004222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VAY0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VAY0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAY0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VAY0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VAY0"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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    {
        "uniprot_canonical_ac": "Q9VB45-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VB45",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 11343.0,
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        "protein_name": "Chitin-binding type-2 domain-containing protein",
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        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB45",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB45"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "chitin binding",
                "id": "GO:0008061",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008061",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VB45",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB45"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [],
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    {
        "uniprot_canonical_ac": "Q9VB48-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB48",
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 127262.0,
        "gene_names": "SD09067p;CG3368;Dmel\\CG3368;Dmel_CG3368;SD09067p",
        "protein_name": "DUF2428 domain-containing protein",
        "disease": [],
        "biological_process": [
            {
                "name": "tRNA nucleoside ribose methylation",
                "id": "GO:0002128",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002128",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB48"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "enzyme regulator activity",
                "id": "GO:0030234",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030234",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB48",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB48"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VB54-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB54",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB54"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 312,
        "chemical_mass": 35199.0,
        "gene_names": "Dmel\\CG14262;CG14262;Dmel\\CG14262;Dmel_CG14262",
        "protein_name": "BTB domain-containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VB71-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB71",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB71"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Dmel\\CG6059;CG6059;Dmel\\CG6059;Dmel_CG6059",
        "protein_name": "Cilia- and flagella-associated protein 58 central coiled coil domain-containing protein",
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            {
                "disease_id": "DOID:0070311",
                "name": "oligoasthenoteratozoospermia",
                "description": "A form of male infertility that is characterized by a combination of low number or oligozoospermia, poor motility or asthenozoospermia, and abnormal shape or teratozoospermia of sperms. OAT is the most common cause of male subfertility.",
                "url": "https://disease-ontology.org/term/DOID:0070311",
                "evidence": [
                    {
                        "id": "0070311",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070311"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0112271",
                "name": "spermatogenic failure 49",
                "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella resulting in markedly reduced or no progressive motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP58 gene on chromosome 10q25.1.",
                "url": "https://disease-ontology.org/term/DOID:0112271",
                "evidence": [
                    {
                        "id": "0112271",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112271"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB71",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB71"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.8"
    },
    {
        "uniprot_canonical_ac": "Q9VB76-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VB76",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VB76"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 311,
        "chemical_mass": 35053.0,
        "gene_names": "CAH9;CAH9;CAIX;CG6074;CT19053;Dmel\\CG6074;Dmel_CG6074;caix",
        "protein_name": "Carbonic anhydrase",
        "disease": [
            {
                "disease_id": "DOID:0050861",
                "name": "colorectal adenocarcinoma",
                "description": "A colorectal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:0050861",
                "evidence": [
                    {
                        "id": "0050861",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050861"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0050997",
                "name": "cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome",
                "description": "A syndrome characterized by congenital onset of nonprogressive cerebellar ataxia, disturbed equilibrium, and mental retardation, associated with cerebellar hypoplasia.",
                "url": "https://disease-ontology.org/term/DOID:0050997",
                "evidence": [
                    {
                        "id": "0050997",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050997"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080199",
                "name": "colorectal carcinoma",
                "description": "A colorectal cancer that arises from the colon or rectum and invades through the muscularis mucosa into the submucosa.",
                "url": "https://disease-ontology.org/term/DOID:0080199",
                "evidence": [
                    {
                        "id": "0080199",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080199"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080365",
                "name": "endometrial hyperplasia",
                "description": "An uterine benign neoplasm that is characterized by excessive proliferation of the cells of the endometrium.",
                "url": "https://disease-ontology.org/term/DOID:0080365",
                "evidence": [
                    {
                        "id": "0080365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080365"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111371",
                "name": "isolated hyperchlorhidrosis",
                "description": "A skin disease characterized by excessive loss of salt in sweat resulting in low levels of salt in the blood in the absence of other symptoms that has_material_basis_in homozygous or compound heterozygous mutation in the CA12 gene on chromosome 15q22.2.",
                "url": "https://disease-ontology.org/term/DOID:0111371",
                "evidence": [
                    {
                        "id": "0111371",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111371"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10584",
                "name": "retinitis pigmentosa",
                "description": "A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss.",
                "url": "https://disease-ontology.org/term/DOID:10584",
                "evidence": [
                    {
                        "id": "10584",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10584"
                    }
                ],
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            },
            {
                "disease_id": "DOID:11054",
                "name": "urinary bladder cancer",
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder.",
                "url": "https://disease-ontology.org/term/DOID:11054",
                "evidence": [
                    {
                        "id": "11054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11054"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2043",
                "name": "hepatitis B",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus (Orthohepadnavirus hominoidei), which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice.",
                "url": "https://disease-ontology.org/term/DOID:2043",
                "evidence": [
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                        "id": "2043",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2043"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:234",
                "name": "colon adenocarcinoma",
                "description": "A colon carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:234",
                "evidence": [
                    {
                        "id": "234",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:234"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2671",
                "name": "transitional cell carcinoma",
                "description": "A carcinoma that derives_from transitional epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:2671",
                "evidence": [
                    {
                        "id": "2671",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2671"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3883",
                "name": "Lynch syndrome",
                "description": "A syndrome that is characterized by an increased risk for colon cancer and cancers of the endometrium, ovary, stomach, small intestine, hepatobiliary tract, urinary tract, brain, and skin and has_material_basis_in mutation of mismatch repair genes that increases the risk of many types of cancers.",
                "url": "https://disease-ontology.org/term/DOID:3883",
                "evidence": [
                    {
                        "id": "3883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3883"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5015",
                "name": "fibrolamellar carcinoma",
                "description": "A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers.",
                "url": "https://disease-ontology.org/term/DOID:5015",
                "evidence": [
                    {
                        "id": "5015",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5015"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
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                ],
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            {
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                "name": "structural constituent of chitin-based cuticle",
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            {
                "name": "plasma membrane",
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                "pmid": ""
            },
            {
                "name": "cell-cell junction",
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                        "id": "Q9VBE5",
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                ],
                "pmid": ""
            },
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                "name": "axon",
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                ],
                "pmid": ""
            },
            {
                "name": "dendrite",
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        ],
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                "name": "neuron remodeling",
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                    {
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            },
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                "name": "neuron projection morphogenesis",
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            },
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                "name": "cell-cell adhesion",
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            },
            {
                "name": "negative regulation of synaptic assembly at neuromuscular junction",
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                    {
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                ],
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        ],
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            {
                "name": "cell adhesion molecule binding",
                "id": "GO:0050839",
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                    {
                        "database": "UniProtKB",
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                ],
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        ],
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                            {
                                "label": "isoglyp",
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                        ],
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                        },
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        ],
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                ],
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    {
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                ],
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        ],
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            {
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                ],
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            {
                "name": "lipid metabolic process",
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            },
            {
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        ],
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            {
                "name": "lipase activity",
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                ],
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            },
            {
                "name": "triacylglycerol lipase activity",
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        ],
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                ],
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                    {
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                ],
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        ],
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            {
                "name": "endoplasmic reticulum membrane",
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                ],
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        ],
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                ],
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                "name": "endoplasmic reticulum",
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            {
                "name": "Golgi apparatus",
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                ],
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                "name": "protein targeting to membrane",
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                "name": "cytosolic ribosome",
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                "name": "cytosolic large ribosomal subunit",
                "id": "GO:0022625",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022625",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VBN5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VBN5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasmic translation",
                "id": "GO:0002181",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002181",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VBN5",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "structural constituent of ribosome",
                "id": "GO:0003735",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003735",
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                    {
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                        "id": "Q9VBN5",
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                    }
                ],
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            }
        ],
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    },
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                    }
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            }
        ],
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        "protein_name": "",
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                "disease_id": "DOID:0050763",
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                "url": "https://disease-ontology.org/term/DOID:0050763",
                "evidence": [
                    {
                        "id": "0050763",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050763"
                    }
                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0070221",
                "evidence": [
                    {
                        "id": "0070221",
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                    }
                ],
                "weight": 0.0
            },
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                "url": "https://disease-ontology.org/term/DOID:0080954",
                "evidence": [
                    {
                        "id": "0080954",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080954"
                    }
                ],
                "weight": 0.0
            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0111353",
                "evidence": [
                    {
                        "id": "0111353",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0111353"
                    }
                ],
                "weight": 0.0
            },
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                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
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                    {
                        "id": "557",
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                        "url": "https://www.alliancegenome.org/disease/DOID:557"
                    }
                ],
                "weight": 0.0
            }
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            {
                "name": "regulation of SNARE complex assembly",
                "id": "GO:0035542",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VBR1",
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                    }
                ],
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            },
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                    }
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                "pmid": ""
            },
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                    }
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            },
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                    }
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            },
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                    }
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                "pmid": ""
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                    }
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            },
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                    }
                ],
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            }
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                    {
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                    }
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            },
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                    }
                ],
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            },
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                    }
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            }
        ],
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                    }
                ],
                "pmid": ""
            }
        ],
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                    }
                ],
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            }
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                "name": "ecdysteroid 22-kinase activity",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                "name": "xenobiotic metabolic process",
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                    }
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            },
            {
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                    }
                ],
                "pmid": ""
            },
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                    }
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                "pmid": ""
            }
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    },
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                        "id": "Q9VC06",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "gene_names": "Dmel\\CG11771;CG11771;Dmel\\CG11771;Dmel_CG11771;anon-EST:Posey100",
        "protein_name": "Peptidase M3A/M3B catalytic domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "mitochondrial intermembrane space",
                "id": "GO:0005758",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005758",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC06"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC06",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VC08-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 754,
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        "gene_names": "Mink;CG11120;Dmel\\CG11120;Dmel_CG11120;Mink;mink",
        "protein_name": "",
        "disease": [],
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            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule binding",
                "id": "GO:0008017",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
                "id": "GO:0005730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005730",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic spindle",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072686",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mitotic chromosome condensation",
                "id": "GO:0007076",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007076",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic cytokinesis",
                "id": "GO:0000281",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000281",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "establishment of mitotic spindle localization",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040001",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC08",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC08"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "Q9VC40-1",
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC40",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC40"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 37974.0,
        "gene_names": "Dmel\\CG5805;CG5805;Dmel\\CG5805;Dmel_CG5805",
        "protein_name": "Solute carrier family 25 member 44",
        "disease": [],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC40",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC40"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC40",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC40"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "branched-chain amino acid catabolic process",
                "id": "GO:0009083",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009083",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VC40",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VC40"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "branched-chain amino acid transport",
                "id": "GO:0015803",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015803",
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                    }
                ],
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            },
            {
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                "evidence": [
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                "name": "mRNA processing",
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                "name": "RNA splicing",
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                "pmid": ""
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                "name": "male mating behavior",
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                "pmid": ""
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                "name": "aminergic neurotransmitter loading into synaptic vesicle",
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        ],
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                "name": "terminal bouton",
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                ],
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                "name": "acyltransferase activity, transferring groups other than amino-acyl groups",
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                ],
                "pmid": ""
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        ],
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                ],
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        ],
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                        "type": "O-linked",
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                            }
                        ],
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                        "site_category_dict": {
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                        },
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                            }
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasm",
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                    }
                ],
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        ],
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                "name": "amino acid metabolic process",
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        ],
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        ],
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                ],
                "pmid": ""
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            {
                "name": "flagellated sperm motility",
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                        "database": "UniProtKB",
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                ],
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            },
            {
                "name": "cilium assembly",
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                "disease_id": "DOID:0111077",
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                "evidence": [
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                ],
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            },
            {
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                    {
                        "id": "10763",
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:12365",
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                ],
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            },
            {
                "name": "potassium ion binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030955",
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                ],
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                "name": "plasma membrane",
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                ],
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                ],
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        ],
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                ],
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        ],
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                "name": "system development",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048731",
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                ],
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            },
            {
                "name": "intracellular protein transport",
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                ],
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                "name": "vesicle-mediated transport",
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                "name": "GTPase activity",
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                    {
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                ],
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                ],
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            {
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                ],
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                "name": "cytoplasm",
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                ],
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            },
            {
                "name": "Golgi apparatus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
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                ],
                "pmid": ""
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        ],
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    {
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                "name": "17-beta-hydroxysteroid dehydrogenase (NADP+) activity",
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                "name": "3-beta-hydroxysteroid 3-dehydrogenase (NADP+) activity",
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                "name": "extracellular space",
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                "name": "circadian rhythm",
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                ],
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                "name": "SRP-dependent cotranslational protein targeting to membrane",
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                ],
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            },
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                "name": "SRP-dependent cotranslational protein targeting to membrane, signal sequence recognition",
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                    {
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                "name": "signal recognition particle, endoplasmic reticulum targeting",
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                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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        ],
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                "name": "DNA-binding transcription factor activity",
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                "name": "transcription cis-regulatory region binding",
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                        "id": "Q9VDQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDQ3"
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                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VDQ3"
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                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
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                        "id": "Q9VDQ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDQ3"
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        ],
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            {
                "name": "regulation of transcription by RNA polymerase II",
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                "pmid": ""
            },
            {
                "name": "positive regulation of gene expression",
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                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
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                ],
                "pmid": ""
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                ],
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                "url": "https://disease-ontology.org/term/DOID:9351",
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                ],
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        ],
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            {
                "name": "plasma membrane",
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        ],
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            {
                "name": "organic anion transport",
                "id": "GO:0015711",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015711",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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            {
                "name": "cytosol",
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        ],
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                "name": "response to oxidative stress",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VDU7"
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                ],
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            {
                "name": "negative regulation of neuron apoptotic process",
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                    {
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                ],
                "pmid": ""
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            {
                "name": "NAD+ biosynthetic process via the salvage pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034355",
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                    {
                        "database": "UniProtKB",
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        ],
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            {
                "name": "calcium ion binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VDU7"
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                ],
                "pmid": ""
            },
            {
                "name": "nicotinamidase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008936",
                "evidence": [
                    {
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                        "id": "Q9VDU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VDU7"
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                ],
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        ],
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                                "id": "40245499",
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                                "url": "https://data.glygen.org/GLY_001163"
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                        ]
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                ]
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                ],
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        ],
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    {
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        "species": [
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                "name": "Drosophila melanogaster",
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                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
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    {
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            {
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                "name": "intracellular sodium ion homeostasis",
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                    {
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                "name": "sodium ion export across plasma membrane",
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            {
                "name": "potassium ion import across plasma membrane",
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                    {
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                    }
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            }
        ],
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            {
                "name": "sodium:potassium-exchanging ATPase complex",
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                    {
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                ],
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                ],
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        ],
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            {
                "name": "cytoplasm",
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                ],
                "pmid": ""
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                "name": "mitochondrion",
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            {
                "name": "mitochondrial matrix",
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                    {
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                        "id": "Q9VEB1",
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                ],
                "pmid": ""
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            {
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                "name": "oxaloacetate metabolic process",
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                "name": "malate-aspartate shuttle",
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                "name": "tRNA wobble adenosine to inosine editing",
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        ],
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                "name": "tRNA-specific adenosine-34 deaminase complex",
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                ],
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                ],
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                "name": "response to oxidative stress",
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                        "end_aa": "Thr",
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                        "evidence": [
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                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
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                    }
                ]
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        ],
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    },
    {
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            {
                "name": "Drosophila melanogaster",
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            }
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            {
                "name": "cilium",
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            },
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                "name": "ciliary base",
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        ],
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                "name": "cilium assembly",
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                ],
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            },
            {
                "name": "intraciliary transport involved in cilium assembly",
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                    {
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            {
                "name": "intraciliary anterograde transport",
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                "name": "intraciliary retrograde transport",
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                    {
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                        "id": "Q9VF41",
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                    }
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        ],
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                ],
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                "disease_id": "DOID:0110467",
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                "url": "https://disease-ontology.org/term/DOID:0110467",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0110831",
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                "url": "https://disease-ontology.org/term/DOID:0110831",
                "evidence": [
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                        "id": "0110831",
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                    }
                ],
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            }
        ],
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            {
                "name": "plasma membrane",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VFH5"
                    }
                ],
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        ],
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                "name": "cell adhesion",
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                        },
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                "name": "synapse assembly",
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                "name": "heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules",
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            {
                "name": "ABC-type transporter activity",
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                    {
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                "pmid": ""
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            {
                "name": "plasma membrane",
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                    {
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                "name": "transmembrane transport",
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            {
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            {
                "name": "response to anoxia",
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                    {
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                        "id": "Q9VGM1",
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                "pmid": ""
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        ],
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                "name": "mitochondrial inner membrane",
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        "disease": [
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11758",
                "name": "iron deficiency anemia",
                "description": "A microcytic anemia that is characterized by pallor, fatigue, lightheadedness, and weakness and has_material_basis_in low total body iron causing impaired synthesis of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:11758",
                "evidence": [
                    {
                        "id": "11758",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11758"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1724",
                "name": "duodenal ulcer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1724",
                "evidence": [
                    {
                        "id": "1724",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1724"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2018",
                "name": "hyperinsulinism",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2018",
                "evidence": [
                    {
                        "id": "2018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "aconitate hydratase activity",
                "id": "GO:0003994",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003994",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "4 iron, 4 sulfur cluster binding",
                "id": "GO:0051539",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051539",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "intracellular iron ion homeostasis",
                "id": "GO:0006879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tricarboxylic acid metabolic process",
                "id": "GO:0072350",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072350",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VGZ3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VGZ3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VH28-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH28",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH28"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 479,
        "chemical_mass": 53789.0,
        "gene_names": "Alp13;Alp13;CG5361;Dmel\\CG5361;Dmel_CG5361",
        "protein_name": "alkaline phosphatase",
        "disease": [],
        "molecular_function": [
            {
                "name": "alkaline phosphatase activity",
                "id": "GO:0004035",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004035",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH28",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH28"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH28",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH28"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH28",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH28"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VH94-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 387,
        "chemical_mass": 44197.0,
        "gene_names": "nmdyn-D7;CG8362;Dmel\\CG8362;Dmel_CG8362;nmdyn-D7",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:10908",
                "name": "hydrocephalus",
                "description": "A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head.",
                "url": "https://disease-ontology.org/term/DOID:10908",
                "evidence": [
                    {
                        "id": "10908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10908"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoside diphosphate kinase activity",
                "id": "GO:0004550",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004550",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "centrosome",
                "id": "GO:0005813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonemal microtubule",
                "id": "GO:0005879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "GTP biosynthetic process",
                "id": "GO:0006183",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006183",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "UTP biosynthetic process",
                "id": "GO:0006228",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006228",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "CTP biosynthetic process",
                "id": "GO:0006241",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006241",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoside triphosphate biosynthetic process",
                "id": "GO:0009142",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009142",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VH94",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VH94"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHA4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 383,
        "chemical_mass": 44398.0,
        "gene_names": "Dmel\\CG8319;CG8319;Dmel\\CG8319;Dmel_CG8319",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "DNA-binding transcription factor activity",
                "id": "GO:0003700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription cis-regulatory region binding",
                "id": "GO:0000976",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000976",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000978",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHA4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHA4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHC0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 374,
        "chemical_mass": 41849.0,
        "gene_names": "RnpS1;CG16788;DEK;Dmel\\CG16788;Dmel_CG16788;RNPS1;RnpS1;Rnps1;cg16788;rnps1",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "mRNA binding",
                "id": "GO:0003729",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003729",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ASAP complex",
                "id": "GO:0061574",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061574",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "RNA splicing",
                "id": "GO:0008380",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008380",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA splicing, via spliceosome",
                "id": "GO:0000398",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000398",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHC0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHC0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VHC0-1",
                "start_pos": "367",
                "end_pos": "367",
                "site_lbl": "Ser367",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "S",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 367,
                        "start_aa": "Ser",
                        "end_pos": 367,
                        "end_aa": "Ser",
                        "residue": "Ser",
                        "site_lbl": "Ser367",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "Q9VHC0",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9VHC0"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHF8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHF8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 265,
        "chemical_mass": 28158.0,
        "gene_names": "SP87;CG12951;Dmel\\CG12951;Dmel_CG12951;SP87",
        "protein_name": "Peptidase S1 domain-containing protein",
        "disease": [
            {
                "disease_id": "DOID:0060074",
                "name": "ductal carcinoma in situ",
                "description": "A breast carcinoma in situ that is characterized by being non-invasive, not having spread outside of the duct into the surrounding breast tissue, has_material_basis_in abnormally proliferating cells, derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:0060074",
                "evidence": [
                    {
                        "id": "0060074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060074"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110057",
                "name": "amelogenesis imperfecta type 2A1",
                "description": "An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the kallikrein-4 gene (KLK4) on chromosome 19q13.",
                "url": "https://disease-ontology.org/term/DOID:0110057",
                "evidence": [
                    {
                        "id": "0110057",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110057"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
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                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:363",
                "name": "uterine cancer",
                "description": "A female reproductive organ cancer that is located_in the uterus.",
                "url": "https://disease-ontology.org/term/DOID:363",
                "evidence": [
                    {
                        "id": "363",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:363"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "serine-type endopeptidase activity",
                "id": "GO:0004252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHF8",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHF8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHF8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHF8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein processing",
                "id": "GO:0016485",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016485",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHF8",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 61385.0,
        "gene_names": "hyx;CDC73;CG11990;Cdc73;Dmel\\CG11990;Dmel_CG11990;Hyrax;Hyx;dCDC73;hyx/CDC73;hyx",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
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                "url": "https://disease-ontology.org/term/DOID:0050866",
                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13543",
                "name": "hyperparathyroidism",
                "description": "A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body.",
                "url": "https://disease-ontology.org/term/DOID:13543",
                "evidence": [
                    {
                        "id": "13543",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13543"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1540",
                "name": "parathyroid carcinoma",
                "description": "An endocrine gland cancer located_in the parathyroid glands located in the neck.",
                "url": "https://disease-ontology.org/term/DOID:1540",
                "evidence": [
                    {
                        "id": "1540",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1540"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2876",
                "name": "laryngeal squamous cell carcinoma",
                "description": "A laryngeal carcinoma that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:2876",
                "evidence": [
                    {
                        "id": "2876",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2876"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5520",
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                "description": "A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck.",
                "url": "https://disease-ontology.org/term/DOID:5520",
                "evidence": [
                    {
                        "id": "5520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5520"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "positive regulation of smoothened signaling pathway",
                "id": "GO:0045880",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045880",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by RNA polymerase II",
                "id": "GO:0045944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of canonical Wnt signaling pathway",
                "id": "GO:0090263",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090263",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription elongation by RNA polymerase II",
                "id": "GO:0006368",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006368",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye morphogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001745",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "chaeta morphogenesis",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing vein morphogenesis",
                "id": "GO:0008586",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008586",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived wing margin morphogenesis",
                "id": "GO:0008587",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008587",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription regulator complex",
                "id": "GO:0005667",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005667",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Cdc73/Paf1 complex",
                "id": "GO:0016593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "RNA polymerase II complex binding",
                "id": "GO:0000993",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000993",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor binding",
                "id": "GO:0140297",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140297",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHI1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VHI1-1",
                "start_pos": "104",
                "end_pos": "104",
                "site_lbl": "Thr104",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 104,
                        "start_aa": "Thr",
                        "end_pos": 104,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr104",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHJ2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 340,
        "chemical_mass": 37947.0,
        "gene_names": "Dmel\\CG11975;CG11975;Dmel\\CG11975;Dmel_CG11975",
        "protein_name": "WD repeat domain phosphoinositide-interacting protein 3",
        "disease": [],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phagophore assembly site membrane",
                "id": "GO:0034045",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034045",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein-macromolecule adaptor activity",
                "id": "GO:0030674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol-3,5-bisphosphate binding",
                "id": "GO:0080025",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0080025",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol-3-phosphate binding",
                "id": "GO:0032266",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032266",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein localization to phagophore assembly site",
                "id": "GO:0034497",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034497",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "autophagy of mitochondrion",
                "id": "GO:0000422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleophagy",
                "id": "GO:0044804",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044804",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycophagy",
                "id": "GO:0061723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pexophagy",
                "id": "GO:0000425",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000425",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHJ2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHJ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHL1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHL1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHL1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 622,
        "chemical_mass": 71658.0,
        "gene_names": "Dmel\\CG9839;CG9839;Dmel\\CG9839;Dmel_CG9839",
        "protein_name": "PiggyBac transposable element-derived protein domain-containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VHM8-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VHM8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VHM8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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                "name": "chemical synaptic transmission",
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                "name": "modulation of chemical synaptic transmission",
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            {
                "name": "presynaptic membrane assembly",
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                "name": "postsynaptic membrane",
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            },
            {
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            {
                "name": "neurexin family protein binding",
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                "name": "signaling receptor activity",
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                "name": "mitochondrion",
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                    {
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                ],
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            },
            {
                "name": "mitochondrial matrix",
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                        "id": "Q9VID7",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "mitochondrial proton-transporting ATP synthase complex assembly",
                "id": "GO:0033615",
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                        "id": "Q9VID7",
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            {
                "name": "protein folding chaperone",
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                    {
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                "name": "nucleotide-excision repair",
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                "name": "telomeric DNA binding",
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                "name": "chromosome, telomeric region",
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        ],
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                "url": "https://disease-ontology.org/term/DOID:0060602",
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                "url": "https://disease-ontology.org/term/DOID:0111068",
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                "disease_id": "DOID:0060230",
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            },
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            }
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                "name": "protein localization to cell surface",
                "id": "GO:0034394",
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                    {
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            {
                "name": "negative regulation of cell fate specification",
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                "name": "sensory organ precursor cell fate determination",
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            {
                "name": "regulation of transcription by RNA polymerase II",
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            {
                "name": "transcription coactivator activity",
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                "disease_id": "DOID:9074",
                "name": "systemic lupus erythematosus",
                "description": "A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart.",
                "url": "https://disease-ontology.org/term/DOID:9074",
                "evidence": [
                    {
                        "id": "9074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9074"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W4R7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4R7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W4R7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4R7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W4R7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4R7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonucleoprotein complex",
                "id": "GO:1990904",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990904",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W4R7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4R7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of gene expression",
                "id": "GO:0010468",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010468",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W4R7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W4R7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q76NS2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q76NS2",
                        "url": "https://www.uniprot.org/uniprotkb/Q76NS2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1029,
        "chemical_mass": 117782.0,
        "gene_names": "Dmel\\CG10353;CG10353;Dmel\\CG10353;Dmel_CG10353",
        "protein_name": "Anoctamin",
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                "disease_id": "DOID:13099",
                "name": "Moyamoya disease",
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                "url": "https://disease-ontology.org/term/DOID:13099",
                "evidence": [
                    {
                        "id": "13099",
                        "database": "AGR",
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                    }
                ],
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            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
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                        "id": "Q76NS2",
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                    }
                ],
                "pmid": ""
            }
        ],
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                "id": "GO:0046983",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046983",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q76NS2",
                        "url": "https://www.uniprot.org/uniprotkb/Q76NS2"
                    }
                ],
                "pmid": ""
            },
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                "name": "intracellularly calcium-gated chloride channel activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005229",
                "evidence": [
                    {
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                        "id": "Q76NS2",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "phospholipid scramblase activity",
                "id": "GO:0017128",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017128",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q76NS2",
                        "url": "https://www.uniprot.org/uniprotkb/Q76NS2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "phospholipid translocation",
                "id": "GO:0045332",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045332",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q76NS2",
                        "url": "https://www.uniprot.org/uniprotkb/Q76NS2"
                    }
                ],
                "pmid": ""
            }
        ],
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        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9W002-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1504,
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        "protein_name": "non-specific serine/threonine protein kinase",
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                "disease_id": "DOID:0081216",
                "name": "autosomal recessive intellectual developmental disorder 54",
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                "url": "https://disease-ontology.org/term/DOID:0081216",
                "evidence": [
                    {
                        "id": "0081216",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081216"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
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                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:2043",
                "name": "hepatitis B",
                "description": "A viral hepatitis that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus (Orthohepadnavirus hominoidei), which is transmitted_by sexual contact, blood transfusions, or fomites like needles or syringes. The infection has_symptom fever, fatigue, loss of appetite, nausea, vomiting, abdominal pain, clay-colored bowel movements, joint pain, and jaundice.",
                "url": "https://disease-ontology.org/term/DOID:2043",
                "evidence": [
                    {
                        "id": "2043",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2043"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "JUN kinase kinase kinase kinase activity",
                "id": "GO:0042656",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042656",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein serine kinase activity",
                "id": "GO:0106310",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0106310",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cell cortex",
                "id": "GO:0005938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005938",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "JNK cascade",
                "id": "GO:0007254",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007254",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to wounding",
                "id": "GO:0009611",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009611",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell shape",
                "id": "GO:0008360",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008360",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "photoreceptor cell morphogenesis",
                "id": "GO:0008594",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008594",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear migration",
                "id": "GO:0007097",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007097",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of embryonic cell shape",
                "id": "GO:0016476",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016476",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "insect visual primordium development",
                "id": "GO:0001748",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001748",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal closure",
                "id": "GO:0007391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "MAPK cascade",
                "id": "GO:0000165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection morphogenesis",
                "id": "GO:0048812",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048812",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tumor necrosis factor-mediated signaling pathway",
                "id": "GO:0033209",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033209",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of Notch signaling pathway",
                "id": "GO:0045746",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045746",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of hippo signaling",
                "id": "GO:0035332",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035332",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of programmed cell death",
                "id": "GO:0043068",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043068",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of MAPK cascade",
                "id": "GO:0043408",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043408",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc fusion, thorax closure",
                "id": "GO:0046529",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046529",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of border follicle cell migration",
                "id": "GO:1903684",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903684",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W002",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W002"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9W002-1",
                "start_pos": "1009",
                "end_pos": "1009",
                "site_lbl": "Thr1009",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1009,
                        "start_aa": "Thr",
                        "end_pos": 1009,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1009",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9W002-1",
                "start_pos": "1090",
                "end_pos": "1090",
                "site_lbl": "Thr1090",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "G49108TO",
                        "type": "O-linked",
                        "subtype": "O-GlcNAcylation",
                        "prediction_tool_list": [],
                        "site_category": "reported_with_glycan",
                        "site_category_dict": {
                            "reported_with_glycan": true
                        },
                        "site_seq": "T",
                        "relation": "attached",
                        "comment": "O-GlcNAcylation",
                        "icn3d_view": {},
                        "start_pos": 1090,
                        "start_aa": "Thr",
                        "end_pos": 1090,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1090",
                        "evidence": [
                            {
                                "id": "40245499",
                                "database": "PubMed",
                                "url": "https://glygen.org/publication/PubMed/40245499"
                            },
                            {
                                "id": "Q9W002",
                                "database": "O-GlcNAc Database",
                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q9W002"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q9W002-1",
                "start_pos": "1167",
                "end_pos": "1167",
                "site_lbl": "Thr1167",
                "weight": 0.0,
                "glycosylation": [
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                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q7KVD1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 2263,
        "chemical_mass": 256976.0,
        "gene_names": "trio;0368/10;03;06];06;0959/14;10;1372/03;1386/06;14;3];BEST:LD36950;CG18214;CG9208;DTrio;Dmel\\CG18214;Dmel_CG18214;M89;TRIO;Trio;UNC-73/Trio;dTrio;l(3)036810;l(3)6D104;l(3)S036810;l(3)S095914;l(3)S137203;l(3)S138606;l(3)S[1372/3];l(3)S[1386/06];l(3)trio;trio",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0061036",
                "name": "autosomal dominant intellectual developmental disorder 63 with macrocephaly",
                "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIO gene on chromosome 5p15.",
                "url": "https://disease-ontology.org/term/DOID:0061036",
                "evidence": [
                    {
                        "id": "0061036",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061036"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070074",
                "name": "autosomal dominant intellectual developmental disorder 44",
                "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TRIO gene on chromosome 5p15.2.",
                "url": "https://disease-ontology.org/term/DOID:0070074",
                "evidence": [
                    {
                        "id": "0070074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070074"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12720",
                "name": "cerebral atherosclerosis",
                "description": "An atherosclerosis of the cerebral vasculature.",
                "url": "https://disease-ontology.org/term/DOID:12720",
                "evidence": [
                    {
                        "id": "12720",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12720"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain.",
                "url": "https://disease-ontology.org/term/DOID:3526",
                "evidence": [
                    {
                        "id": "3526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3526"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "regulation of axonogenesis",
                "id": "GO:0050770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050770",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "central nervous system development",
                "id": "GO:0007417",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007417",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin cytoskeleton organization",
                "id": "GO:0030036",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030036",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of Rho protein signal transduction",
                "id": "GO:0035025",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035025",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of synaptic assembly at neuromuscular junction",
                "id": "GO:0045887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon guidance",
                "id": "GO:0007411",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon target recognition",
                "id": "GO:0007412",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007412",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived leg morphogenesis",
                "id": "GO:0007480",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007480",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mushroom body development",
                "id": "GO:0016319",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016319",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "axon",
                "id": "GO:0030424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "growth cone",
                "id": "GO:0030426",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030426",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extrinsic component of cytoplasmic side of plasma membrane",
                "id": "GO:0031234",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031234",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extrinsic component of membrane",
                "id": "GO:0019898",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019898",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "guanyl-nucleotide exchange factor activity",
                "id": "GO:0005085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinase activity",
                "id": "GO:0016301",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016301",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVD1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVD1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q7KVD1-1",
                "start_pos": "1675",
                "end_pos": "1675",
                "site_lbl": "Thr1675",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1675,
                        "start_aa": "Thr",
                        "end_pos": 1675,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1675",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VQQ6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 458,
        "chemical_mass": 52195.0,
        "gene_names": "Snx1;CG2774;Dmel\\CG2774;Dmel_CG2774;Dsnx1;Snx1;Vps5;snx1",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "endosome",
                "id": "GO:0005768",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005768",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "early endosome membrane",
                "id": "GO:0031901",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031901",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell projection",
                "id": "GO:0042995",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042995",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "retromer, tubulation complex",
                "id": "GO:0030905",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030905",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endomembrane system",
                "id": "GO:0012505",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012505",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endosome membrane",
                "id": "GO:0010008",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010008",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "retrograde transport, endosome to Golgi",
                "id": "GO:0042147",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042147",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endocytic recycling",
                "id": "GO:0032456",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032456",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "early endosome to Golgi transport",
                "id": "GO:0034498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "phosphatidylinositol-3-phosphate binding",
                "id": "GO:0032266",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032266",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphatidylinositol binding",
                "id": "GO:0035091",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035091",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VQQ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VQQ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9W3R9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1000,
        "chemical_mass": 109053.0,
        "gene_names": "Dmel\\CG1677;CG1677;Dmel\\CG1677;Dmel_CG1677",
        "protein_name": "C3H1-type domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-macromolecule adaptor activity",
                "id": "GO:0030674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA cap binding complex binding",
                "id": "GO:0140262",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140262",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mRNA splicing, via spliceosome",
                "id": "GO:0000398",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000398",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA destabilization",
                "id": "GO:0050779",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050779",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "catalytic step 2 spliceosome",
                "id": "GO:0071013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "precatalytic spliceosome",
                "id": "GO:0071011",
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                    }
                ],
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            },
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                "name": "actin filament binding",
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            }
        ],
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                    }
                ],
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            },
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                "name": "cell periphery",
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                "name": "ruffle",
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                    }
                ],
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                    }
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                "pmid": ""
            },
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                "name": "Z disc",
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                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "cell adhesion",
                "id": "GO:0007155",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VSL8"
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                "pmid": ""
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                "name": "negative regulation of DNA-templated transcription",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VSL8"
                    }
                ],
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            {
                "name": "cell adhesion mediated by integrin",
                "id": "GO:0033627",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron differentiation",
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                        "id": "Q9VSL8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSL8"
                    }
                ],
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            },
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                "name": "sarcomere organization",
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                    }
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                "pmid": ""
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                "name": "cardiac muscle cell-cardiac muscle cell adhesion",
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                        "id": "Q9VSL8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSL8"
                    }
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                "pmid": ""
            },
            {
                "name": "muscle attachment",
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                        "id": "Q9VSL8",
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                    }
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                "name": "actin cytoskeleton organization",
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                "name": "cell-cell adhesion",
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                "name": "terminal branching, open tracheal system",
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                ],
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            },
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                "name": "lumen formation, open tracheal system",
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                "name": "somatic muscle attachment to chitin-based cuticle",
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                    {
                        "database": "UniProtKB",
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                    }
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                "name": "Drosophila melanogaster",
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                ],
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        ],
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            {
                "name": "lateral plasma membrane",
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                    }
                ],
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            {
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                    }
                ],
                "pmid": ""
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        ],
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                "name": "open tracheal system development",
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                ],
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            {
                "name": "septate junction assembly",
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                    }
                ],
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            {
                "name": "dorsal trunk growth, open tracheal system",
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                    }
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            {
                "name": "regulation of tube size, open tracheal system",
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                        "url": "https://www.uniprot.org/uniprotkb/Q7KT16"
                    }
                ],
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            },
            {
                "name": "regulation of tube length, open tracheal system",
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q7KT16"
                    }
                ],
                "pmid": ""
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                ],
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        ],
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                "name": "ATP binding",
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                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
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                        "id": "Q0E8F2",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP transmembrane transporter activity",
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                "evidence": [
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                        "id": "Q0E8F2",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "mitochondrial inner membrane",
                "id": "GO:0005743",
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                        "database": "UniProtKB",
                        "id": "Q0E8F2",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
                    }
                ],
                "pmid": ""
            }
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                "name": "ADP transport",
                "id": "GO:0015866",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015866",
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                        "database": "UniProtKB",
                        "id": "Q0E8F2",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
                    }
                ],
                "pmid": ""
            },
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                "name": "ATP transport",
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                        "database": "UniProtKB",
                        "id": "Q0E8F2",
                        "url": "https://www.uniprot.org/uniprotkb/Q0E8F2"
                    }
                ],
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            },
            {
                "name": "transmembrane transport",
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                        "id": "Q0E8F2",
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                    }
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            }
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                    {
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                    {
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                            {
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                        "sequence_org": "D",
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                            {
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                            {
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                            {
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                            {
                                "database": "UniProtKB",
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    {
        "uniprot_canonical_ac": "Q7KTL5-1",
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                    {
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                        "id": "Q7KTL5",
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                ],
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        ],
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            {
                "name": "mitotic cytokinesis",
                "id": "GO:0000281",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000281",
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                    {
                        "database": "UniProtKB",
                        "id": "Q7KTL5",
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            },
            {
                "name": "intracellular protein localization",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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                ],
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                    {
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            },
            {
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                ],
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            }
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            {
                "name": "nucleus",
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                    {
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                "pmid": ""
            }
        ],
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                "name": "zinc ion binding",
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                    {
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            },
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            },
            {
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                    {
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                    {
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                ],
                "pmid": ""
            }
        ],
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    {
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                    {
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                            {
                                "label": "isoglyp",
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                        ],
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                        "site_category_dict": {
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                        },
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                        "evidence": [
                            {
                                "id": "40245499",
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                            {
                                "id": "Q7KTB0",
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                                "url": "https://www.oglcnac.mcw.edu/search/?query_protein=Q7KTB0"
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                            {
                                "id": "33925313",
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    {
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        "protein_name": "",
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                "url": "https://disease-ontology.org/term/DOID:0080581",
                "evidence": [
                    {
                        "id": "0080581",
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            {
                "name": "ATP binding",
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                        "id": "Q9VL02",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
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                    {
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                        "id": "Q9VL02",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane protein dislocase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VL02",
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                    }
                ],
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        ],
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            {
                "name": "mitochondrial outer membrane",
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            },
            {
                "name": "extraction of mislocalized protein from mitochondrial outer membrane",
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                    {
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                    }
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            }
        ],
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                ],
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        "gene_names": "Dmel\\CG34325;CG18358;CG34325;Dmel\\CG34325;Dmel_CG34325",
        "protein_name": "LIM zinc-binding domain-containing protein",
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                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coregulator activity",
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                    {
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                        "id": "Q9VXC1",
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                    }
                ],
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            }
        ],
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                        "id": "Q9VXC1",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "Z disc",
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                "pmid": ""
            },
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                "name": "anchoring junction",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                        "database": "UniProtKB",
                        "id": "Q86B94",
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                ],
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        ],
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        "gene_names": "mfas;7;87A7-9/7;BEST:GH06752;CG3359;Dmel\\CG3359;Dmel_CG3359;FBgn0260745;Mfas;anon-87Af;anon-EST:Liang-97;anon-WO0140519.174;clone 97;gh06752;mfas",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0060444",
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                "url": "https://disease-ontology.org/term/DOID:0060444",
                "evidence": [
                    {
                        "id": "0060444",
                        "database": "AGR",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:0060447",
                "name": "epithelial basement membrane dystrophy",
                "description": "An epithelial and subepithelial dystrophy that is characterized by sheet-like areas of basement membrane originating from the basal epithelial cells of the corneal epithelium and extending superficially into the epithelium.",
                "url": "https://disease-ontology.org/term/DOID:0060447",
                "evidence": [
                    {
                        "id": "0060447",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0060447"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060453",
                "name": "Reis-Bucklers corneal dystrophy",
                "description": "An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and irregular geographic opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, and has_material_basis_in heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption especially of Bowman's membrane of the cornea.",
                "url": "https://disease-ontology.org/term/DOID:0060453",
                "evidence": [
                    {
                        "id": "0060453",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060453"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060455",
                "name": "Thiel-Behnke corneal dystrophy",
                "description": "An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and honeycomb-shaped opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption especially of Bowman's membrane of the cornea.",
                "url": "https://disease-ontology.org/term/DOID:0060455",
                "evidence": [
                    {
                        "id": "0060455",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060455"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080010",
                "name": "bone structure disease",
                "description": "A bone disease that has_material_basis_in an abnormality in the location or function of the skeletal structure.",
                "url": "https://disease-ontology.org/term/DOID:0080010",
                "evidence": [
                    {
                        "id": "0080010",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080010"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080530",
                "name": "granular corneal dystrophy 1",
                "description": "A granular corneal dystrophy that is characterized by recurrent erosions and gray crumb-like opacification located_in the cornea, proteinaceous rock candy-like deposits in the anterior stroma and subepithelium, and progressive vision loss later in life as deposits move into the central vision, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption of the corneal surface.",
                "url": "https://disease-ontology.org/term/DOID:0080530",
                "evidence": [
                    {
                        "id": "0080530",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080530"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1474",
                "name": "aggressive periodontitis",
                "description": "A periodontitis that is characterized by rapid attachment loss and bone destruction in the presence of little local factors such as dental plaque and dental calculus resulting in inflammation and a loss of periodontium.",
                "url": "https://disease-ontology.org/term/DOID:1474",
                "evidence": [
                    {
                        "id": "1474",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1474"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2566",
                "name": "corneal dystrophy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2566",
                "evidence": [
                    {
                        "id": "2566",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2566"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:557",
                "name": "kidney disease",
                "description": "A urinary system disease that is located_in the kidney.",
                "url": "https://disease-ontology.org/term/DOID:557",
                "evidence": [
                    {
                        "id": "557",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:557"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7693",
                "name": "abdominal aortic aneurysm",
                "description": "An aortic aneurysm that is located_in the abdominal aorta.",
                "url": "https://disease-ontology.org/term/DOID:7693",
                "evidence": [
                    {
                        "id": "7693",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7693"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:784",
                "name": "chronic kidney disease",
                "description": "A kidney failure that is characterized by the gradual loss of kidney function, present for a minimum of 3 months. CKD is classified based on cause, glomerular filtration rate (GFR) category (G2-G5), and albuminuria category (A1-A3).",
                "url": "https://disease-ontology.org/term/DOID:784",
                "evidence": [
                    {
                        "id": "784",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:784"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:824",
                "name": "periodontitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:824",
                "evidence": [
                    {
                        "id": "824",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:824"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:90",
                "name": "degenerative disc disease",
                "description": "A bone deterioration disease that has_material_basis_in gradual dehydration and tears located_in intervertebral disc.",
                "url": "https://disease-ontology.org/term/DOID:90",
                "evidence": [
                    {
                        "id": "90",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:90"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:971",
                "name": "tendinitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:971",
                "evidence": [
                    {
                        "id": "971",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:971"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonogenesis",
                "id": "GO:0007409",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007409",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix organization",
                "id": "GO:0030198",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030198",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of hemocyte proliferation",
                "id": "GO:0035207",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035207",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cell adhesion molecule binding",
                "id": "GO:0050839",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050839",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q86B94",
                        "url": "https://www.uniprot.org/uniprotkb/Q86B94"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q86B94-1",
                "start_pos": "563",
                "end_pos": "563",
                "site_lbl": "Thr563",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 563,
                        "start_aa": "Thr",
                        "end_pos": 563,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr563",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "M9ND65-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9ND65",
                        "url": "https://www.uniprot.org/uniprotkb/M9ND65"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 705,
        "chemical_mass": 82488.0,
        "gene_names": "Dmel\\CG16854;CG16854;Dmel\\CG16854;Dmel_CG16854;gi7297815",
        "protein_name": "DUF229 domain containing protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q7KVX1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVX1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVX1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 443,
        "chemical_mass": 48876.0,
        "gene_names": "Pdha1;CG 7010;CG7010;Dmel\\CG7010;Dmel_CG7010;E1-PDH;L(1)G0334;L(1)g0334;PDH-E1;PDHA1;PDHE1;PDHalpha;PDH;Pdha[KK101856];Pdha;Pdh;l (1) G0334;l(1)G0334;pdha",
        "protein_name": "Pyruvate dehydrogenase E1 component subunit alpha",
        "disease": [
            {
                "disease_id": "DOID:0014667",
                "name": "disease of metabolism",
                "description": "A disease that involves errors in metabolic processes of building or degradation of molecules.",
                "url": "https://disease-ontology.org/term/DOID:0014667",
                "evidence": [
                    {
                        "id": "0014667",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0014667"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070569",
                "name": "spermatogenic failure 70",
                "description": "A spermatogenic failure characterized by azoospermia or sperm immotility and necrozoospermia that has_material_basis_in homozygous mutation in the PDHA2 gene on chromosome 4q22.3.",
                "url": "https://disease-ontology.org/term/DOID:0070569",
                "evidence": [
                    {
                        "id": "0070569",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070569"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3649",
                "name": "pyruvate decarboxylase deficiency",
                "description": "A carbohydrate metabolic disorder characterized by the buildup of lactic acid in the body and a variety of neurological problems and caused by a deficiency of one of the three enzymes in the pyruvate dehydrogenase complex.",
                "url": "https://disease-ontology.org/term/DOID:3649",
                "evidence": [
                    {
                        "id": "3649",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3649"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8466",
                "name": "retinal degeneration",
                "description": "A retinal disease that is characterized by deterioration of the retina caused by the progressive and eventual death of the cells of the retina.",
                "url": "https://disease-ontology.org/term/DOID:8466",
                "evidence": [
                    {
                        "id": "8466",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8466"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVX1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVX1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pyruvate dehydrogenase complex",
                "id": "GO:0045254",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045254",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVX1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVX1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "pyruvate dehydrogenase (acetyl-transferring) activity",
                "id": "GO:0004739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVX1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVX1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "pyruvate decarboxylation to acetyl-CoA",
                "id": "GO:0006086",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006086",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q7KVX1",
                        "url": "https://www.uniprot.org/uniprotkb/Q7KVX1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1ZAH6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAH6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAH6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 577,
        "chemical_mass": 65074.0,
        "gene_names": "Dmel\\CG4945;CG4945;CT15864;Dmel\\CG4945;Dmel_CG4945;PKN",
        "protein_name": "Protein kinase domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAH6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAH6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAH6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAH6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mesoderm development",
                "id": "GO:0007498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAH6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAH6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1Z9B0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9B0",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9B0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 674,
        "chemical_mass": 78137.0,
        "gene_names": "Dmel\\CG4712;CG4712;Dmel\\CG4712;Dmel_CG4712",
        "protein_name": "CCDC113/CCDC96 coiled-coil domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "cilium",
                "id": "GO:0005929",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005929",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9B0",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9B0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axoneme",
                "id": "GO:0005930",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9B0",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9B0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ciliary basal body",
                "id": "GO:0036064",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036064",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9B0",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9B0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cilium assembly",
                "id": "GO:0060271",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060271",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9B0",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9B0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
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                "name": "oligopeptide transport",
                "id": "GO:0006857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006857",
                "evidence": [
                    {
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                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dipeptide import across plasma membrane",
                "id": "GO:0140206",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140206",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dipeptide transmembrane transporter activity",
                "id": "GO:0071916",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071916",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "X2JCG8",
                        "url": "https://www.uniprot.org/uniprotkb/X2JCG8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "X2JCG8-1",
                "start_pos": "50",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
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                    }
                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "Q8I0K9-1",
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            {
                "name": "Drosophila melanogaster",
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                ],
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        ],
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        "protein_name": "Tektin",
        "disease": [
            {
                "disease_id": "DOID:0070580",
                "name": "spermatogenic failure 81",
                "description": "A spermatogenic failure characterized by oligoasthenoteratozoospermia with acrosomal hypoplasia and detachment of the acrosome from the sperm head that has_material_basis_in homozygous or compound heterozygous mutation in the TEKT3 gene on chromosome 17p12.",
                "url": "https://disease-ontology.org/term/DOID:0070580",
                "evidence": [
                    {
                        "id": "0070580",
                        "database": "AGR",
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                    }
                ],
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            }
        ],
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            {
                "name": "cilium movement involved in cell motility",
                "id": "GO:0060294",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060294",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "flagellated sperm motility",
                "id": "GO:0030317",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030317",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cilium assembly",
                "id": "GO:0060271",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060271",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule nucleation",
                "id": "GO:0007020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cilium",
                "id": "GO:0005929",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005929",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule cytoskeleton",
                "id": "GO:0015630",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015630",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axoneme",
                "id": "GO:0005930",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of cytoskeleton",
                "id": "GO:0005200",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005200",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q8I0K9",
                        "url": "https://www.uniprot.org/uniprotkb/Q8I0K9"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "O76876-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 53395.0,
        "gene_names": "ssx;CG3056;Dmel\\CG3056;Dmel_CG3056;EG:132E8.1;Ssx;anon-EST:Posey102;cg3056;ssx",
        "protein_name": "Protein sex-lethal",
        "disease": [],
        "molecular_function": [
            {
                "name": "mRNA binding",
                "id": "GO:0003729",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003729",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA 3'-UTR binding",
                "id": "GO:0003730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003730",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "poly(A) binding",
                "id": "GO:0008143",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008143",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "poly(U) RNA binding",
                "id": "GO:0008266",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008266",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "defense response to bacterium",
                "id": "GO:0042742",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042742",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sex differentiation",
                "id": "GO:0007548",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007548",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of signal transduction",
                "id": "GO:0009967",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009967",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of RNA splicing",
                "id": "GO:0043484",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043484",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "post-transcriptional gene silencing",
                "id": "GO:0016441",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016441",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of mRNA processing",
                "id": "GO:0050686",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050686",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonucleoprotein complex",
                "id": "GO:1990904",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990904",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "O76876",
                        "url": "https://www.uniprot.org/uniprotkb/O76876"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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            {
                "uniprot_canonical_ac": "O76876-1",
                "start_pos": "482",
                "end_pos": "482",
                "site_lbl": "Thr482",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 482,
                        "start_aa": "Thr",
                        "end_pos": 482,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr482",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VWJ6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 214503.0,
        "gene_names": "rictor;8002;CG8002;Dmel\\CG8002;Dmel_CG8002;RICTOR;Rictor;dRICTOR;dRictor;dRic;rictor",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050861",
                "name": "colorectal adenocarcinoma",
                "description": "A colorectal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:0050861",
                "evidence": [
                    {
                        "id": "0050861",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050861"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3007",
                "name": "breast ductal carcinoma",
                "description": "A breast carcinoma that derives_from the lining of milk ducts.",
                "url": "https://disease-ontology.org/term/DOID:3007",
                "evidence": [
                    {
                        "id": "3007",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3007"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3121",
                "name": "gallbladder cancer",
                "description": "A biliary tract cancer that is located_in the gallbladder.",
                "url": "https://disease-ontology.org/term/DOID:3121",
                "evidence": [
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                        "id": "3121",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3121"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3319",
                "name": "lymphangioleiomyomatosis",
                "description": "A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas.",
                "url": "https://disease-ontology.org/term/DOID:3319",
                "evidence": [
                    {
                        "id": "3319",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3319"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3748",
                "name": "esophagus squamous cell carcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial squamous cells located_in the esophagus.",
                "url": "https://disease-ontology.org/term/DOID:3748",
                "evidence": [
                    {
                        "id": "3748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5409",
                "name": "lung small cell carcinoma",
                "description": "A lung carcinoma that has_material_basis_in primitive-appearing cells that are smaller than normal cells and is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:5409",
                "evidence": [
                    {
                        "id": "5409",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5409"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8649",
                "name": "tongue cancer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8649",
                "evidence": [
                    {
                        "id": "8649",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8649"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "TOR signaling",
                "id": "GO:0031929",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031929",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dendrite morphogenesis",
                "id": "GO:0048813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to starvation",
                "id": "GO:0009267",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009267",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "stress granule assembly",
                "id": "GO:0034063",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034063",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of dendrite development",
                "id": "GO:0050773",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050773",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cell size",
                "id": "GO:0008361",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008361",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to insulin stimulus",
                "id": "GO:0032869",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032869",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction",
                "id": "GO:0051897",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051897",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein localization to nucleus",
                "id": "GO:0034504",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034504",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of cell size",
                "id": "GO:0045793",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045793",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of insulin receptor signaling pathway",
                "id": "GO:0046628",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046628",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of synaptic assembly at neuromuscular junction",
                "id": "GO:0045887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "TORC2 signaling",
                "id": "GO:0038203",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0038203",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by transcription factor localization",
                "id": "GO:0061586",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061586",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "TORC2 complex",
                "id": "GO:0031932",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031932",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activator activity",
                "id": "GO:0043539",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043539",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q0KHS0-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 819,
        "chemical_mass": 91692.0,
        "gene_names": "kat80;CG13956;CG9910;Dmel\\CG13956;Dmel_CG13956;KATNB1;Kat-80;Kat80;Katanin80;kat-80;kat80",
        "protein_name": "Katanin p80 WD40 repeat-containing subunit B1",
        "disease": [
            {
                "disease_id": "DOID:0060250",
                "name": "idiopathic scoliosis",
                "description": "A scoliosis with no known cause.",
                "url": "https://disease-ontology.org/term/DOID:0060250",
                "evidence": [
                    {
                        "id": "0060250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060250"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112236",
                "name": "lissencephaly 6",
                "description": "A microlissencephaly characterized by severe microcephaly, developmental delay, lissencephaly, pachygyria, and hypoplasia of the corpus callosum that has_material_basis_in homozygous or compound heterozygous mutation in the KATNB1 gene on chromosome 16q21.",
                "url": "https://disease-ontology.org/term/DOID:0112236",
                "evidence": [
                    {
                        "id": "0112236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10907",
                "name": "microcephaly",
                "description": "A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.",
                "url": "https://disease-ontology.org/term/DOID:10907",
                "evidence": [
                    {
                        "id": "10907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10907"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "microtubule severing",
                "id": "GO:0051013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell division",
                "id": "GO:0051301",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051301",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal appendage formation",
                "id": "GO:0046843",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046843",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule depolymerization",
                "id": "GO:0007019",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007019",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "katanin complex",
                "id": "GO:0008352",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008352",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "spindle pole",
                "id": "GO:0000922",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000922",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "centrosome",
                "id": "GO:0005813",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005813",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "microtubule binding",
                "id": "GO:0008017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q0KHS0",
                        "url": "https://www.uniprot.org/uniprotkb/Q0KHS0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "R9PY37-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "R9PY37",
                        "url": "https://www.uniprot.org/uniprotkb/R9PY37"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 939,
        "chemical_mass": 101271.0,
        "gene_names": "smal;CG13986;CG13987;CG13988;CG15813;CG31640;CG34380;Dmel\\CG34380;Dmel_CG34380;anon-WO0073329.6;smal",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050156",
                "name": "idiopathic pulmonary fibrosis",
                "description": "A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe.",
                "url": "https://disease-ontology.org/term/DOID:0050156",
                "evidence": [
                    {
                        "id": "0050156",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050156"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050866",
                "name": "oral squamous cell carcinoma",
                "description": "An oral cavity cancer that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:0050866",
                "evidence": [
                    {
                        "id": "0050866",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050866"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112196",
                "name": "spondylometaepiphyseal dysplasia, short limb-hand type",
                "description": "A spondyloepimetaphyseal dysplasia characterized by short stature, short limbs and hands, and typical radiological features which include platyspondyly, metaphyseal, and epiphyseal involvement, short tubular bones of the limbs, and abnormal calcification of cartilage that has_material_basis_in homozygous or compound heterozygous mutation in the DDR2 gene on chromosome 1q23.3.",
                "url": "https://disease-ontology.org/term/DOID:0112196",
                "evidence": [
                    {
                        "id": "0112196",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112196"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14018",
                "name": "alcoholic liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14018",
                "evidence": [
                    {
                        "id": "14018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3070",
                "name": "high grade glioma",
                "description": "A cell type cancer that has_material_basis_in glial cells and is located in brain or located in spine.",
                "url": "https://disease-ontology.org/term/DOID:3070",
                "evidence": [
                    {
                        "id": "3070",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3070"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3347",
                "name": "osteosarcoma",
                "description": "A bone sarcoma that is located_in bone that has_material_basis_in cells of mesenchymal origin. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus).",
                "url": "https://disease-ontology.org/term/DOID:3347",
                "evidence": [
                    {
                        "id": "3347",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3347"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3500",
                "name": "gallbladder adenocarcinoma",
                "description": "A gallbladder carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3500",
                "evidence": [
                    {
                        "id": "3500",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3500"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3907",
                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.",
                "url": "https://disease-ontology.org/term/DOID:3907",
                "evidence": [
                    {
                        "id": "3907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3907"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4467",
                "name": "clear cell renal cell carcinoma",
                "description": "A renal cell carcinoma that has_material_basis_in cells that appear very pale or clear when examined under microscope.",
                "url": "https://disease-ontology.org/term/DOID:4467",
                "evidence": [
                    {
                        "id": "4467",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4467"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5520",
                "name": "head and neck squamous cell carcinoma",
                "description": "A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck.",
                "url": "https://disease-ontology.org/term/DOID:5520",
                "evidence": [
                    {
                        "id": "5520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5520"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5627",
                "name": "adenosquamous gallbladder carcinoma",
                "description": "A gallbladder carcinoma that derives_from squamous cells and gland-like cells.",
                "url": "https://disease-ontology.org/term/DOID:5627",
                "evidence": [
                    {
                        "id": "5627",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5627"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
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            {
                "name": "central nervous system development",
                "id": "GO:0007417",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007417",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonal fasciculation",
                "id": "GO:0007413",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007413",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin biosynthetic process",
                "id": "GO:0006031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dorsal closure",
                "id": "GO:0007391",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007391",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "open tracheal system development",
                "id": "GO:0007424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007424",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based embryonic cuticle biosynthetic process",
                "id": "GO:0008362",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008362",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of tube size, open tracheal system",
                "id": "GO:0035151",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035151",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "UDP-N-acetylglucosamine biosynthetic process",
                "id": "GO:0006048",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006048",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of axon guidance",
                "id": "GO:1902669",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902669",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "UDP-N-acetylglucosamine diphosphorylase activity",
                "id": "GO:0003977",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003977",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y0Z0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y0Z0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VWQ7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 163,
        "chemical_mass": 18560.0,
        "gene_names": "Dmel\\CG6891;CG6891;Cotl1;Dmel\\CG6891;Dmel_CG6891",
        "protein_name": "Coactosin-like protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "actin binding",
                "id": "GO:0003779",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament binding",
                "id": "GO:0051015",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051015",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cortical actin cytoskeleton",
                "id": "GO:0030864",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030864",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "site of polarized growth",
                "id": "GO:0030427",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030427",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of actin filament polymerization",
                "id": "GO:0030833",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030833",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VWQ7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VWQ7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "E1JIM6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1015,
        "chemical_mass": 111179.0,
        "gene_names": "ss;AHR;AhR;CG6993;Dmel\\CG6993;Dmel_CG6993;SS;Ss;dAHR;ssa;ss",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050741",
                "name": "alcohol dependence",
                "description": "A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol.",
                "url": "https://disease-ontology.org/term/DOID:0050741",
                "evidence": [
                    {
                        "id": "0050741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081292",
                "name": "traumatic brain injury",
                "description": "A brain disease that is characterized by brain dysfunction caused by an outside force, usually a violent blow to the head.",
                "url": "https://disease-ontology.org/term/DOID:0081292",
                "evidence": [
                    {
                        "id": "0081292",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081292"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112142",
                "name": "retinitis pigmentosa 85",
                "description": "A retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in AHR on chromosome 7p21.1.",
                "url": "https://disease-ontology.org/term/DOID:0112142",
                "evidence": [
                    {
                        "id": "0112142",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112142"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11984",
                "name": "hypertrophic cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.",
                "url": "https://disease-ontology.org/term/DOID:11984",
                "evidence": [
                    {
                        "id": "11984",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11984"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9649",
                "name": "congenital nystagmus",
                "description": "A pathologic nystagmus, present at birth, characterized by involuntary, rhythmic eye movements; oscillations are usually horizontal in direction.",
                "url": "https://disease-ontology.org/term/DOID:9649",
                "evidence": [
                    {
                        "id": "9649",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9649"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "male courtship behavior",
                "id": "GO:0008049",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008049",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "specification of animal organ identity",
                "id": "GO:0010092",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010092",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of transcription by RNA polymerase II",
                "id": "GO:0000122",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000122",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "memory",
                "id": "GO:0007613",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007613",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription by RNA polymerase II",
                "id": "GO:0045944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of dendrite morphogenesis",
                "id": "GO:0048814",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048814",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "xenobiotic metabolic process",
                "id": "GO:0006805",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006805",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular receptor signaling pathway",
                "id": "GO:0030522",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030522",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "antennal development",
                "id": "GO:0007469",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007469",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "imaginal disc-derived leg segmentation",
                "id": "GO:0036011",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036011",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "antennal morphogenesis",
                "id": "GO:0048800",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048800",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of R7 cell differentiation",
                "id": "GO:0045676",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045676",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "R7 cell differentiation",
                "id": "GO:0045466",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045466",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein heterodimerization activity",
                "id": "GO:0046982",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046982",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription cis-regulatory region binding",
                "id": "GO:0000976",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000976",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear receptor activity",
                "id": "GO:0004879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "aryl hydrocarbon receptor complex",
                "id": "GO:0034751",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034751",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JIM6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JIM6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
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    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VK22"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 649,
        "chemical_mass": 73707.0,
        "gene_names": "kek4;CG9431;CT26742;Dmel\\CG9431;Dmel_CG9431;kek-4;kek4",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0111628",
                "name": "high myopia-sensorineural deafness syndrome",
                "description": "A syndrome characterized by severe myopia and moderate to profound, bilateral, progressive sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the SLITRK6 gene on chromosome 13q31.1.",
                "url": "https://disease-ontology.org/term/DOID:0111628",
                "evidence": [
                    {
                        "id": "0111628",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111628"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK22",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK22"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VK63-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK63",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK63"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 799,
        "chemical_mass": 89094.0,
        "gene_names": "Dmel\\CG5776;CG5776;Dmel\\CG5776;Dmel_CG5776",
        "protein_name": "AAA+ ATPase domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK63",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK63"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK63",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK63"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK63",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK63"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "ribosomal large subunit biogenesis",
                "id": "GO:0042273",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042273",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK63",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK63"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
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    },
    {
        "uniprot_canonical_ac": "Q9VK84-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 745,
        "chemical_mass": 83119.0,
        "gene_names": "Oatp33Ea;CG5427;Dmel\\CG5427;Dmel_CG5427;EcI-2;Oatp33Ea;oatp 33Ea",
        "protein_name": "Solute carrier organic anion transporter family member",
        "disease": [
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12236",
                "name": "primary biliary cholangitis",
                "description": "A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts.",
                "url": "https://disease-ontology.org/term/DOID:12236",
                "evidence": [
                    {
                        "id": "12236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12308",
                "name": "Dubin-Johnson syndrome",
                "description": "A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin without elevation of liver alanine transaminase and aspartate transaminase enzymes as a result of the deficient ability of hepatocytes to secrete conjugated bilirubin into the bile.",
                "url": "https://disease-ontology.org/term/DOID:12308",
                "evidence": [
                    {
                        "id": "12308",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12308"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13580",
                "name": "cholestasis",
                "description": "A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum.",
                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14283",
                "name": "primary hypertrophic osteoarthropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14283",
                "evidence": [
                    {
                        "id": "14283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1520",
                "name": "colon carcinoma",
                "description": "A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:1520",
                "evidence": [
                    {
                        "id": "1520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1520"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
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                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2741",
                "name": "bilirubin metabolic disorder",
                "description": "An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.",
                "url": "https://disease-ontology.org/term/DOID:2741",
                "evidence": [
                    {
                        "id": "2741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2998",
                "name": "testicular cancer",
                "description": "A male reproductive system cancer that is located_in the testicles.",
                "url": "https://disease-ontology.org/term/DOID:2998",
                "evidence": [
                    {
                        "id": "2998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3007",
                "name": "breast ductal carcinoma",
                "description": "A breast carcinoma that derives_from the lining of milk ducts.",
                "url": "https://disease-ontology.org/term/DOID:3007",
                "evidence": [
                    {
                        "id": "3007",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3007"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3571",
                "name": "liver cancer",
                "description": "A hepatobiliary system cancer that is located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:3571",
                "evidence": [
                    {
                        "id": "3571",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3571"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:9253",
                "name": "gastrointestinal stromal tumor",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9253",
                "evidence": [
                    {
                        "id": "9253",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9253"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9452",
                "name": "steatotic liver disease",
                "description": "A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in at least 5% of hepatocytes.",
                "url": "https://disease-ontology.org/term/DOID:9452",
                "evidence": [
                    {
                        "id": "9452",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9452"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "monoatomic ion transport",
                "id": "GO:0006811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "organic anion transport",
                "id": "GO:0015711",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015711",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium-independent organic anion transport",
                "id": "GO:0043252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VK84",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VK84"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VKB3-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 39377.0,
        "gene_names": "Mt2;CG10692;DNMT2;DNMT;DmMT2;Dmel\\CG10692;Dmel_CG10692;Dnmt2;Dnmt;Mt2;dDNMT2;dDNMT;dDnmt2;dnmt2;nmt2",
        "protein_name": "tRNA (cytosine(38)-C(5))-methyltransferase",
        "disease": [],
        "molecular_function": [
            {
                "name": "DNA (cytosine-5-)-methyltransferase activity",
                "id": "GO:0003886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA methyltransferase activity",
                "id": "GO:0008175",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008175",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA (cytidine-5-)-methyltransferase activity",
                "id": "GO:0016428",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016428",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA binding",
                "id": "GO:0000049",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000049",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "methyltransferase activity",
                "id": "GO:0008168",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008168",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "epigenetic programming of gene expression",
                "id": "GO:0043045",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043045",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "subtelomeric heterochromatin formation",
                "id": "GO:0031509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006338",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to oxidative stress",
                "id": "GO:0006979",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006979",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA processing",
                "id": "GO:0008033",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008033",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of defense response to virus by host",
                "id": "GO:0002230",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002230",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "response to heat",
                "id": "GO:0009408",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009408",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA methylation",
                "id": "GO:0030488",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030488",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "determination of adult lifespan",
                "id": "GO:0008340",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008340",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of innate immune response",
                "id": "GO:0045089",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045089",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA methylation-dependent constitutive heterochromatin formation",
                "id": "GO:0006346",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006346",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of tRNA stability",
                "id": "GO:0036415",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0036415",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transposable element silencing by heterochromatin formation",
                "id": "GO:0141005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0141005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
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                        "id": "Q9VKB3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic stress granule",
                "id": "GO:0010494",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010494",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VKB3"
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                ],
                "pmid": ""
            },
            {
                "name": "chromosome, telomeric region",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000781",
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                    {
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                ],
                "pmid": ""
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        ],
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                "evidence": [
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                ],
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                ],
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            {
                "name": "protein insertion into mitochondrial outer membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045040",
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                "pmid": ""
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            {
                "name": "protein insertion into mitochondrial inner membrane",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "protein targeting to mitochondrion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006626",
                "evidence": [
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VKC8"
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                "pmid": ""
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            {
                "name": "protein import into mitochondrial matrix",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030150",
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                    {
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                "pmid": ""
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        ],
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                "name": "mitochondrial outer membrane",
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            },
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                "name": "mitochondrial outer membrane translocase complex",
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            {
                "name": "mitochondrion targeting sequence binding",
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                "pmid": ""
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        ],
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                "name": "cytosol",
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        ],
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                "name": "catalytic activity",
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            },
            {
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        ],
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            },
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                ],
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                ],
                "pmid": ""
            },
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                "name": "neuron projection",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
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                "name": "dynein axonemal particle",
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            {
                "name": "nervous system development",
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                "evidence": [
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                ],
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            },
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                "name": "cilium movement",
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            },
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                "name": "axonemal dynein complex assembly",
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                ],
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            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
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        ],
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            {
                "name": "cytokine activity",
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                ],
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        ],
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    {
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                ],
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        ],
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        "gene_names": "Dmel\\CG6700;CG6700;Dmel\\CG6700;Dmel_CG6700",
        "protein_name": "PCI domain-containing protein",
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            {
                "name": "nucleus",
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                ],
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            },
            {
                "name": "mating",
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        ],
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                "name": "serine hydrolase activity",
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                "pmid": ""
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                "name": "extracellular region",
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        ],
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                "name": "melanization defense response",
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        ],
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            {
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            },
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            {
                "name": "regulation of transcription by RNA polymerase II",
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                ],
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                ],
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                ],
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            },
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                "name": "Rab GDP-dissociation inhibitor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005093",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "GDP-dissociation inhibitor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005092",
                "evidence": [
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                "pmid": ""
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        ],
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            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                        "database": "UniProtKB",
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                ],
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                "name": "synaptic vesicle",
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        ],
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
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                ],
                "pmid": ""
            },
            {
                "name": "small GTPase-mediated signal transduction",
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            },
            {
                "name": "vesicle-mediated transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016192",
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            },
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                "id": "GO:0007269",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007269",
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                ],
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        ],
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                ],
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        ],
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            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                ],
                "pmid": ""
            },
            {
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                ],
                "pmid": ""
            }
        ],
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                ],
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        ],
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                ],
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        ],
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            {
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                    {
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                        "id": "Q9VLL4",
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                ],
                "pmid": ""
            }
        ],
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            {
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
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                        "id": "Q9VLL4",
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                ],
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            }
        ],
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            {
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                "id": "GO:0008543",
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                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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                ],
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        ],
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                "disease_id": "DOID:0110178",
                "name": "Charcot-Marie-Tooth disease axonal type 2V",
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                    {
                        "id": "0110178",
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                "disease_id": "DOID:0111394",
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                "evidence": [
                    {
                        "id": "0111394",
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                ],
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                ],
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                        "id": "12801",
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                ],
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            }
        ],
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            {
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            },
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLL5",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "heparin proteoglycan metabolic process",
                "id": "GO:0030202",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030202",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLL5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLL5"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "alpha-N-acetylglucosaminidase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLL5",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "lysosomal lumen",
                "id": "GO:0043202",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043202",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLL5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLL5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "vacuole",
                "id": "GO:0005773",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005773",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLL5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLL5"
                    }
                ],
                "pmid": ""
            }
        ],
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                "start_pos": "738",
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                "site_lbl": "Thr738",
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                    {
                        "glytoucan_ac": "",
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                            {
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                        ]
                    }
                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VLR3-1",
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            {
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                        "id": "Q9VLR3",
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                ],
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            }
        ],
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                "disease_id": "DOID:10534",
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                "description": "A gastrointestinal system cancer that is located_in the stomach.",
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                ],
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            },
            {
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                        "database": "AGR",
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                    }
                ],
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            }
        ],
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            {
                "name": "cytidine deaminase activity",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLR3",
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                    }
                ],
                "pmid": ""
            },
            {
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                "evidence": [
                    {
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                        "id": "Q9VLR3",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "identical protein binding",
                "id": "GO:0042802",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042802",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLR3",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
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                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLR3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "nucleobase-containing small molecule metabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055086",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLR3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "pyrimidine-containing compound metabolic process",
                "id": "GO:0072527",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072527",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLR3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
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                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VLV3",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "chemical_mass": 42996.0,
        "gene_names": "Spn28Db;CG12318;CG33121;Dmel\\CG33121;Dmel_CG33121;Spn28Db",
        "protein_name": "",
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            {
                "disease_id": "DOID:0050589",
                "name": "inflammatory bowel disease",
                "description": "An intestinal disease characterized by inflammation located in all parts of digestive tract.",
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                    {
                        "id": "0050589",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050589"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0050831",
                "name": "familial encephalopathy with neuroserpin inclusion bodies",
                "description": "A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern.",
                "url": "https://disease-ontology.org/term/DOID:0050831",
                "evidence": [
                    {
                        "id": "0050831",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050831"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0051054",
                "name": "coarctation of the aorta",
                "description": "A congenital heart disease that is characterized by the luminal narrowing of the thoracic aortic arch, typically located just beyond the left subclavian artery. This narrowing creates an obstruction that can lead to significant cardiovascular complications, including systemic hypertension, left ventricular hypertrophy, and eventually heart failure.",
                "url": "https://disease-ontology.org/term/DOID:0051054",
                "evidence": [
                    {
                        "id": "0051054",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051054"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060186",
                "name": "chemical colitis",
                "description": "A colitis caused_by introduction of various chemicals.",
                "url": "https://disease-ontology.org/term/DOID:0060186",
                "evidence": [
                    {
                        "id": "0060186",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060186"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060189",
                "name": "ileitis",
                "description": "An inflammatory bowel disease characterized by inflammation located_in ileum, has_symptom diarrhea, has_symptom abdominal pain, often in the right lower quadrant, has_symptom weight loss.",
                "url": "https://disease-ontology.org/term/DOID:0060189",
                "evidence": [
                    {
                        "id": "0060189",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060189"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060224",
                "name": "atrial fibrillation",
                "description": "A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain.",
                "url": "https://disease-ontology.org/term/DOID:0060224",
                "evidence": [
                    {
                        "id": "0060224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060224"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060903",
                "name": "thrombosis",
                "description": "A vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system.",
                "url": "https://disease-ontology.org/term/DOID:0060903",
                "evidence": [
                    {
                        "id": "0060903",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060903"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070555",
                "name": "Nagashima-type palmoplantar keratosis",
                "description": "A nonepidermolytic palmoplantar keratoderma characterized by mild, well-demarcated, diffuse erythematous hyperkeratosis that is nonprogressive after the second decade of life which extends onto the dorsal surfaces of the palms and feet and the Achilles tendon area, with a high frequency of hyperhidrosis on the palms and soles and without flexion contractures or constricting bands that has_material_basis_in homozygous or compound heterozygous mutation in the SERPINB7 gene on chromosome 18q21.33.",
                "url": "https://disease-ontology.org/term/DOID:0070555",
                "evidence": [
                    {
                        "id": "0070555",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070555"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090030",
                "name": "corticosteroid-binding globulin deficiency",
                "description": "An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32.",
                "url": "https://disease-ontology.org/term/DOID:0090030",
                "evidence": [
                    {
                        "id": "0090030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10159",
                "name": "osteonecrosis",
                "description": "An ischemic bone disease that results_in necrosis located_in bone.",
                "url": "https://disease-ontology.org/term/DOID:10159",
                "evidence": [
                    {
                        "id": "10159",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10159"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10591",
                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10952",
                "name": "nephritis",
                "description": "A kidney disease that is characterized by an inflammation of the kidneys.",
                "url": "https://disease-ontology.org/term/DOID:10952",
                "evidence": [
                    {
                        "id": "10952",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10952"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11111",
                "name": "hydronephrosis",
                "description": "An urinary system disease that is characterized by swelling of one or both kidneys due to incomplete voiding of urine.",
                "url": "https://disease-ontology.org/term/DOID:11111",
                "evidence": [
                    {
                        "id": "11111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11123",
                "name": "IgA vasculitis",
                "description": "A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.",
                "url": "https://disease-ontology.org/term/DOID:11123",
                "evidence": [
                    {
                        "id": "11123",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11123"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11247",
                "name": "disseminated intravascular coagulation",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11247",
                "evidence": [
                    {
                        "id": "11247",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11247"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11394",
                "name": "adult respiratory distress syndrome",
                "description": "A respiratory failure that results from diffuse injury to the endothelium of the lung (as in sepsis, chest trauma, massive blood transfusion, aspiration of the gastric contents, or pneumonia) and is characterized by pulmonary edema with an abnormally high amount of protein in the edematous fluid and by difficult rapid breathing and hypoxemia.",
                "url": "https://disease-ontology.org/term/DOID:11394",
                "evidence": [
                    {
                        "id": "11394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11396",
                "name": "pulmonary edema",
                "description": "A respiratory failure that is characterized by the accumulation of fluid in the lung tissues causing disturbance of the gas exchange that may lead to respiratory failure.",
                "url": "https://disease-ontology.org/term/DOID:11396",
                "evidence": [
                    {
                        "id": "11396",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11396"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
                "description": "A nephrosis characterized by marked increase in glomerular protein permeability resulting in marked elevation of urine protein levels, hypoalbuminemia, hyperlipidemia, and hypercoagulability.",
                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11949",
                "name": "Creutzfeldt-Jakob disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11949",
                "evidence": [
                    {
                        "id": "11949",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11949"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11984",
                "name": "hypertrophic cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.",
                "url": "https://disease-ontology.org/term/DOID:11984",
                "evidence": [
                    {
                        "id": "11984",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11984"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1205",
                "name": "allergic disease",
                "description": "An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods.",
                "url": "https://disease-ontology.org/term/DOID:1205",
                "evidence": [
                    {
                        "id": "1205",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1205"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12185",
                "name": "otosclerosis",
                "description": "An otitis interna characterized by isolated endochondral bone sclerosis of the labyrinthine capsule.",
                "url": "https://disease-ontology.org/term/DOID:12185",
                "evidence": [
                    {
                        "id": "12185",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12185"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12351",
                "name": "alcoholic hepatitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:12351",
                "evidence": [
                    {
                        "id": "12351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13372",
                "name": "alpha 1-antitrypsin deficiency",
                "description": "A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells.",
                "url": "https://disease-ontology.org/term/DOID:13372",
                "evidence": [
                    {
                        "id": "13372",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13372"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13884",
                "name": "sick sinus syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13884",
                "evidence": [
                    {
                        "id": "13884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13884"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14115",
                "name": "toxic shock syndrome",
                "description": "A commensal bacterial infectious disease that results_in infection, has_material_basis_in Streptococcus pyogenes or has_material_basis_in Staphylococcus aureus, which produce toxins that are absorbed systemically and produce the systemic manifestations. The infection has_symptom fever, has_symptom rash, has_symptom hypotension, has_symptom multiorgan failure, has_symptom desquamation, has_symptom vomiting, has_symptom diarrhea, has_symptom headache, and has_symptom nonfocal neurologic abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:14115",
                "evidence": [
                    {
                        "id": "14115",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14115"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14499",
                "name": "Fabry disease",
                "description": "A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.",
                "url": "https://disease-ontology.org/term/DOID:14499",
                "evidence": [
                    {
                        "id": "14499",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14499"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1580",
                "name": "diffuse scleroderma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1580",
                "evidence": [
                    {
                        "id": "1580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2018",
                "name": "hyperinsulinism",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2018",
                "evidence": [
                    {
                        "id": "2018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2349",
                "name": "arteriosclerosis",
                "description": "An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:2349",
                "evidence": [
                    {
                        "id": "2349",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2349"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2377",
                "name": "multiple sclerosis",
                "description": "A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.",
                "url": "https://disease-ontology.org/term/DOID:2377",
                "evidence": [
                    {
                        "id": "2377",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2377"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2913",
                "name": "acute pancreatitis",
                "description": "A pancreatitis that is characterized by inflammation of the pancreas over a short period of time and has symptoms of severe abdominal pain, nausea, vomiting, diarrhea, fever, and shock.",
                "url": "https://disease-ontology.org/term/DOID:2913",
                "evidence": [
                    {
                        "id": "2913",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2913"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2945",
                "name": "severe acute respiratory syndrome",
                "description": "A Coronavirus infectious disease that results_in infection located_in respiratory tract, has_material_basis_in Severe acute respiratory syndrome coronavirus (SARS-CoV or SARS-CoV-1), a subtype of Betacoronavirus pandemicum, which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia.",
                "url": "https://disease-ontology.org/term/DOID:2945",
                "evidence": [
                    {
                        "id": "2945",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2945"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3021",
                "name": "acute kidney failure",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3021",
                "evidence": [
                    {
                        "id": "3021",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3021"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3407",
                "name": "carotid artery disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3407",
                "evidence": [
                    {
                        "id": "3407",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3407"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3587",
                "name": "pancreatic ductal carcinoma",
                "description": "A pancreatic carcinoma located_in the pancreatic duct.",
                "url": "https://disease-ontology.org/term/DOID:3587",
                "evidence": [
                    {
                        "id": "3587",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3587"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3755",
                "name": "antithrombin III deficiency",
                "description": "A thrombophilia that is characterized by the tendency to form clots in the veins.",
                "url": "https://disease-ontology.org/term/DOID:3755",
                "evidence": [
                    {
                        "id": "3755",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3755"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3910",
                "name": "lung adenocarcinoma",
                "description": "A lung non-small cell carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3910",
                "evidence": [
                    {
                        "id": "3910",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3910"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:409",
                "name": "liver disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:409",
                "evidence": [
                    {
                        "id": "409",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:409"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4724",
                "name": "brain edema",
                "description": "A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.",
                "url": "https://disease-ontology.org/term/DOID:4724",
                "evidence": [
                    {
                        "id": "4724",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4724"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5082",
                "name": "liver cirrhosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5082",
                "evidence": [
                    {
                        "id": "5082",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5082"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6432",
                "name": "pulmonary hypertension",
                "description": "A hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries.",
                "url": "https://disease-ontology.org/term/DOID:6432",
                "evidence": [
                    {
                        "id": "6432",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6432"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6713",
                "name": "cerebrovascular disease",
                "description": "An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain.",
                "url": "https://disease-ontology.org/term/DOID:6713",
                "evidence": [
                    {
                        "id": "6713",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6713"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8398",
                "name": "osteoarthritis",
                "description": "An arthritis that has_material_basis_in worn out cartilage located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:8398",
                "evidence": [
                    {
                        "id": "8398",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8398"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8552",
                "name": "chronic myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by over production of white blood cells.",
                "url": "https://disease-ontology.org/term/DOID:8552",
                "evidence": [
                    {
                        "id": "8552",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8552"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:865",
                "name": "vasculitis",
                "description": "A vascular disease that is characterized by inflammation of the blood vessels.",
                "url": "https://disease-ontology.org/term/DOID:865",
                "evidence": [
                    {
                        "id": "865",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:865"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8805",
                "name": "intermediate coronary syndrome",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8805",
                "evidence": [
                    {
                        "id": "8805",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8805"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8923",
                "name": "skin melanoma",
                "description": "A skin cancer that has_material_basis_in melanocytes.",
                "url": "https://disease-ontology.org/term/DOID:8923",
                "evidence": [
                    {
                        "id": "8923",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8923"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8947",
                "name": "diabetic retinopathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:8947",
                "evidence": [
                    {
                        "id": "8947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9675",
                "name": "pulmonary emphysema",
                "description": "A chronic obstructive pulmonary disease that is characterized by permanent enlargement of air spaces distal to the terminal bronchioles and the destruction of the alveolar walls.",
                "url": "https://disease-ontology.org/term/DOID:9675",
                "evidence": [
                    {
                        "id": "9675",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9675"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:988",
                "name": "mitral valve prolapse",
                "description": "A mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole.",
                "url": "https://disease-ontology.org/term/DOID:988",
                "evidence": [
                    {
                        "id": "988",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:988"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLV3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLV3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "mating",
                "id": "GO:0007618",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007618",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLV3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLV3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VLW1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLW1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLW1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 265,
        "chemical_mass": 29930.0,
        "gene_names": "lectin-28C;AC 004723A;AC004723a;CG7106;Dmel\\CG7106;Dmel_CG7106;lectin-28C",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLW1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLW1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "carbohydrate binding",
                "id": "GO:0030246",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030246",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLW1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLW1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "galactose binding",
                "id": "GO:0005534",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005534",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLW1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLW1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "opsonization",
                "id": "GO:0008228",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008228",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLW1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLW1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VLX5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLX5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLX5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 696,
        "chemical_mass": 78119.0,
        "gene_names": "Dmel\\CG7179;CG7179;CT22169;Dmel\\CG7179;Dmel_CG7179;Opa;anon-28Cg;tld-like",
        "protein_name": "CUB domain-containing protein",
        "disease": [],
        "molecular_function": [
            {
                "name": "hydrolase activity",
                "id": "GO:0016787",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016787",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLX5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLX5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "synaptic target recognition",
                "id": "GO:0008039",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008039",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLX5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLX5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VLY4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 595,
        "chemical_mass": 68519.0,
        "gene_names": "Dmel\\CG13794;CG13794;Dmel\\CG13794;Dmel_CG13794",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "neurotransmitter transmembrane transporter activity",
                "id": "GO:0005326",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005326",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neurotransmitter:sodium symporter activity",
                "id": "GO:0005328",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005328",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycine:sodium symporter activity",
                "id": "GO:0015375",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015375",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "amino acid transport",
                "id": "GO:0006865",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006865",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transmembrane transport",
                "id": "GO:0035725",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035725",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neurotransmitter transport",
                "id": "GO:0006836",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006836",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q9VLY4-1",
                "start_pos": "272",
                "end_pos": "272",
                "site_lbl": "Thr272",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 272,
                        "start_aa": "Thr",
                        "end_pos": 272,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr272",
                        "evidence": [
                            {
                                "id": "GLY_001163",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/GLY_001163"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VLY5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 583,
        "chemical_mass": 66966.0,
        "gene_names": "Dmel\\CG13793;CG13793;Dmel\\CG13793;Dmel_CG13793",
        "protein_name": "Transporter",
        "disease": [],
        "molecular_function": [
            {
                "name": "neurotransmitter transmembrane transporter activity",
                "id": "GO:0005326",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005326",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neurotransmitter:sodium symporter activity",
                "id": "GO:0005328",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005328",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glycine:sodium symporter activity",
                "id": "GO:0015375",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015375",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "amino acid transport",
                "id": "GO:0006865",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006865",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VLY5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VLY5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transmembrane transport",
                "id": "GO:0035725",
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                ],
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                "name": "double-strand break repair via homologous recombination",
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                "name": "mitotic intra-S DNA damage checkpoint signaling",
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            {
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                ],
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            },
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                "description": "",
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                "evidence": [
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                "disease_id": "DOID:11335",
                "name": "sarcoidosis",
                "description": "A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs.",
                "url": "https://disease-ontology.org/term/DOID:11335",
                "evidence": [
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                "url": "https://disease-ontology.org/term/DOID:14250",
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                ],
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                "name": "cystic fibrosis",
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                        "id": "1485",
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                        "id": "1580",
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                ],
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                        "id": "2378",
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                        "id": "2797",
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                "url": "https://disease-ontology.org/term/DOID:2841",
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                        "id": "2841",
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                ],
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                ],
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                "name": "plasma membrane",
                "id": "GO:0005886",
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                ],
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        ],
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 34083.0,
        "gene_names": "Osi18;CG1169;Dmel\\CG1169;Dmel_CG1169;Osi18;osi18",
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            {
                "name": "plasma membrane",
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        ],
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                ],
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        ],
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        ],
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                ],
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        ],
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            {
                "name": "cytoplasm",
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                "name": "Hsp90 protein binding",
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                "name": "multivesicular body fusion to apical plasma membrane",
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                "url": "https://disease-ontology.org/term/DOID:14502",
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                "name": "positive regulation of apoptotic process",
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                "name": "determination of adult lifespan",
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            {
                "name": "tetrapyrrole metabolic process",
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        ],
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                "name": "glutamate-gated calcium ion channel activity",
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                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
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            {
                "name": "glutamate receptor activity",
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                "name": "ionotropic glutamate receptor complex",
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                "name": "synapse",
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                "name": "neuromuscular synaptic transmission",
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            {
                "name": "serine-type endopeptidase activity",
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                        "id": "4989",
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                    }
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                "url": "https://disease-ontology.org/term/DOID:784",
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                        "id": "784",
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                "url": "https://disease-ontology.org/term/DOID:9351",
                "evidence": [
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                        "id": "9351",
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                        "id": "9352",
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                    }
                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:9970",
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                        "id": "9970",
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            }
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            {
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                "id": "GO:0005615",
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                    {
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                        "id": "Q9VS66",
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                "pmid": ""
            }
        ],
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                    {
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                ],
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            }
        ],
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                    {
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            }
        ],
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            }
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                    }
                ],
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            },
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                "evidence": [
                    {
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                        "database": "AGR",
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                    }
                ],
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            }
        ],
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            },
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            },
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                "name": "dendrite membrane",
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                ],
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                    }
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        ],
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                "name": "detection of temperature stimulus involved in sensory perception of pain",
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            },
            {
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                ],
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            },
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                    }
                ],
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            },
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                ],
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        ],
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            {
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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        ],
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            {
                "name": "structural constituent of cuticle",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                ],
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        ],
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                "name": "cilium movement involved in cell motility",
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                ],
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            },
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "inner dynein arm assembly",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "sperm flagellum",
                "id": "GO:0036126",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "inner dynein arm",
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                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "dynein light chain binding",
                "id": "GO:0045503",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045503",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VS90"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dynein heavy chain binding",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VS90",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VS90"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VSC6-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Pop4;BcDNA:LD45688;CG8038;Dmel\\CG8038;Dmel_CG8038;Pop4;Rpp29;anon-WO0172774.38",
        "protein_name": "Ribonuclease P protein subunit p29",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleolar ribonuclease P complex",
                "id": "GO:0005655",
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                "evidence": [
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "multimeric ribonuclease P complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030681",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleus",
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                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonuclease MRP complex",
                "id": "GO:0000172",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000172",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ribonuclease P complex",
                "id": "GO:0030677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030677",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "RNA processing",
                "id": "GO:0006396",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006396",
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                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA processing",
                "id": "GO:0008033",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008033",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "rRNA processing",
                "id": "GO:0006364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006364",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA 5'-leader removal",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001682",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "ribonuclease P RNA binding",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "rRNA primary transcript binding",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VSC6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSC6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
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                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "Q9VSE8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSE8"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 441,
        "chemical_mass": 50241.0,
        "gene_names": "Uxs;CG7979;Dmel\\CG7979;Dmel_CG7979;Uxs",
        "protein_name": "UDP-glucuronic acid decarboxylase 1",
        "disease": [],
        "biological_process": [
            {
                "name": "D-xylose metabolic process",
                "id": "GO:0042732",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042732",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VSE8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VSE8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "UDP-D-xylose biosynthetic process",
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            },
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                "name": "SCF ubiquitin ligase complex",
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    {
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            {
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                "name": "cytoplasmic microtubule organization",
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            {
                "name": "mitotic spindle-templated microtubule nucleation",
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                "name": "spindle pole",
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                "name": "centrosome",
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                "name": "microtubule",
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                "name": "gamma-tubulin complex",
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                "name": "gamma-tubulin ring complex",
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                "name": "positive regulation of DNA-templated transcription",
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                "name": "mesodermal cell fate commitment",
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                "name": "carbohydrate metabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005975",
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            {
                "name": "UDP-N-acetylglucosamine biosynthetic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006048",
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                "name": "trachea development",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060438",
                "evidence": [
                    {
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            {
                "name": "mitochondrial inner membrane",
                "id": "GO:0005743",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005743",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "respiratory chain complex I",
                "id": "GO:0045271",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045271",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
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                "pmid": ""
            }
        ],
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            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "2 iron, 2 sulfur cluster binding",
                "id": "GO:0051537",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051537",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "oxidoreductase activity",
                "id": "GO:0016491",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016491",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NADH dehydrogenase (ubiquinone) activity",
                "id": "GO:0008137",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008137",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVF0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVF0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "mitochondrial electron transport, NADH to ubiquinone",
                "id": "GO:0006120",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006120",
                "evidence": [
                    {
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                        "id": "Q9VVF0",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                        "id": "Q9VVF2",
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        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                    }
                ],
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            }
        ],
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            {
                "name": "actin binding",
                "id": "GO:0003779",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phospholipid binding",
                "id": "GO:0005543",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005543",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "endosome",
                "id": "GO:0005768",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005768",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin cytoskeleton",
                "id": "GO:0015629",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015629",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosomal membrane",
                "id": "GO:0005765",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005765",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "membrane organization",
                "id": "GO:0061024",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0061024",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell projection assembly",
                "id": "GO:0030031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030031",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVG1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVG1"
                    }
                ],
                "pmid": ""
            }
        ],
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        "record_id": "batch.fruitfly.9"
    },
    {
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        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "chemical_mass": 29248.0,
        "gene_names": "Ndfip;CG32177;CG8056;Dmel\\CG32177;Dmel_CG32177;Ndfip;anon-EST:Liang-2.19;clone 2.19;dNdfip",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "vacuolar transport",
                "id": "GO:0007034",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007034",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of Notch signaling pathway",
                "id": "GO:0045747",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045747",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of protein ubiquitination",
                "id": "GO:0031398",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031398",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin-dependent protein catabolic process",
                "id": "GO:0006511",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006511",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of Notch signaling pathway",
                "id": "GO:0045746",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045746",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion transport",
                "id": "GO:0030001",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030001",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "wing disc development",
                "id": "GO:0035220",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035220",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "endoplasmic reticulum",
                "id": "GO:0005783",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005783",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perinuclear region of cytoplasm",
                "id": "GO:0048471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "late endosome",
                "id": "GO:0005770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005770",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin ligase complex",
                "id": "GO:0000151",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000151",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "WW domain binding",
                "id": "GO:0050699",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050699",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVJ5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVJ5"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS1"
                    }
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        ],
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                "url": "https://disease-ontology.org/term/DOID:0060475",
                "evidence": [
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                        "id": "0060475",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060475"
                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0060536",
                "evidence": [
                    {
                        "id": "0060536",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060536"
                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0070329",
                "evidence": [
                    {
                        "id": "0070329",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070329"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "mitochondrial DNA depletion syndrome 19",
                "description": "A mitochondrial DNA depletion syndrome that has_material_basis_in compound heterozygous mutation in the SLC25A10 gene on chromosome 17q25.3.",
                "url": "https://disease-ontology.org/term/DOID:0070450",
                "evidence": [
                    {
                        "id": "0070450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070450"
                    }
                ],
                "weight": 0.0
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        ],
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                        "database": "UniProtKB",
                        "id": "Q9VVS1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS1"
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                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial inner membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005743",
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                        "id": "Q9VVS1",
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                    }
                ],
                "pmid": ""
            },
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                "name": "membrane",
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                        "id": "Q9VVS1",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS1"
                    }
                ],
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        ],
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                "name": "sulfate transmembrane transport",
                "id": "GO:1902358",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902358",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VVS1",
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                    }
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            },
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                        "id": "Q9VVS1",
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                        "id": "Q9VVS1",
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                    }
                ],
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            },
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                ],
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            }
        ],
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS6"
                    }
                ],
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        ],
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        "protein_name": "Ubiquitin-like-conjugating enzyme ATG3",
        "disease": [],
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                "name": "autophagosome assembly",
                "id": "GO:0000045",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000045",
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                        "database": "UniProtKB",
                        "id": "Q9VVS6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
                "evidence": [
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                        "id": "Q9VVS6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VVS6"
                    }
                ],
                "pmid": ""
            },
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                "name": "macroautophagy",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016236",
                "evidence": [
                    {
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                ],
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                "name": "metal ion binding",
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                ],
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        ],
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                                "label": "isoglyp",
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                        ],
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                        },
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                            }
                        ]
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                ]
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    },
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                "name": "Drosophila melanogaster",
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "PMP34;BcDNA:RE36975;CG1326;CG32250;Dmel\\CG32250;Dmel_CG32250;PMP34;Pmp34;SLC25A17;dPMP34",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "peroxisomal membrane",
                "id": "GO:0005778",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005778",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZD9",
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                "pmid": ""
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        ],
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            {
                "name": "transmembrane transporter activity",
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                    {
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                        "id": "Q9VZD9",
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                "pmid": ""
            },
            {
                "name": "ATP transmembrane transporter activity",
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                        "id": "Q9VZD9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZD9"
                    }
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                "pmid": ""
            },
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                "name": "ADP transmembrane transporter activity",
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                        "id": "Q9VZD9",
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            },
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                "name": "coenzyme A transmembrane transporter activity",
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                "disease_id": "DOID:0111399",
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                "description": "A congenital dyserythropoietic anemia characterized by nonprogressive mild to moderate hemolytic anemia, macrocytosis in the peripheral blood, intravascular hemolysis, and giant multinucleated erythroblasts in the bone marrow and that has_material_basis_in heterozygous mutation in the KIF23 gene on chromosome 15q23.",
                "url": "https://disease-ontology.org/term/DOID:0111399",
                "evidence": [
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                    }
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                "name": "kinetochore microtubule",
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            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule",
                "id": "GO:0005874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinesin complex",
                "id": "GO:0005871",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005871",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cleavage furrow",
                "id": "GO:0032154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axoneme",
                "id": "GO:0005930",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "midbody",
                "id": "GO:0030496",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030496",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "contractile ring",
                "id": "GO:0070938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070938",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "centralspindlin complex",
                "id": "GO:0097149",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097149",
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic spindle midzone",
                "id": "GO:1990023",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990023",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
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                ],
                "pmid": ""
            },
            {
                "name": "male germline ring canal",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035323",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "somatic ring canal",
                "id": "GO:0098549",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098549",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "female germline ring canal",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035324",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "maintenance of protein location in cell",
                "id": "GO:0032507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "somatic muscle development",
                "id": "GO:0007525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007525",
                "evidence": [
                    {
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                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of canonical Wnt signaling pathway",
                "id": "GO:0090090",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090090",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "peripheral nervous system development",
                "id": "GO:0007422",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007422",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic cytokinesis",
                "id": "GO:0000281",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000281",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule-based movement",
                "id": "GO:0007018",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007018",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell fate determination",
                "id": "GO:0001709",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001709",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic spindle organization",
                "id": "GO:0007052",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007052",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitotic spindle midzone assembly",
                "id": "GO:0051256",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051256",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of microtubule cytoskeleton organization",
                "id": "GO:0070507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actomyosin contractile ring contraction",
                "id": "GO:0000916",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000916",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule sliding",
                "id": "GO:0051012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of neuron projection arborization",
                "id": "GO:0150013",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0150013",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "larval somatic muscle development",
                "id": "GO:0007526",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007526",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule binding",
                "id": "GO:0008017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP hydrolysis activity",
                "id": "GO:0016887",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016887",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microtubule motor activity",
                "id": "GO:0003777",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003777",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZF5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZF5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9VZK7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "Q9VZK7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZK7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 773,
        "chemical_mass": 84833.0,
        "gene_names": "Dmel\\CG14982;CG14982;Dmel\\CG14982;Dmel_CG14982",
        "protein_name": "Centrosome-associated FAM110 C-terminal domain-containing protein",
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            {
                "uniprot_canonical_ac": "Q9VZK7-1",
                "start_pos": "481",
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                "site_lbl": "Thr481",
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                    {
                        "glytoucan_ac": "",
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                        "subtype": "",
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                                "label": "isoglyp",
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                            }
                        ],
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                        "site_category_dict": {
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                        },
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                            }
                        ]
                    }
                ]
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            {
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                        ],
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                        },
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                                "id": "GLY_001163",
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                        ]
                    }
                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "Q9VZK8-1",
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                "name": "Drosophila melanogaster",
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                        "id": "Q9VZK8",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 36458.0,
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        "protein_name": "NADP-dependent oxidoreductase domain-containing protein",
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        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZK8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZK8"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "aldose reductase (NADPH) activity",
                "id": "GO:0004032",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004032",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZK8",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZK8"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
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        ],
        "length": 302,
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        "gene_names": "Tecr;CG10849;Dmel\\CG10849;Dmel_CG10849;SC2;Sc2;Ter[CG10849];dSc2;l(3)05634;l(3)63Eb;l(3)SH4",
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            {
                "disease_id": "DOID:0050889",
                "name": "non-syndromic intellectual disability",
                "description": "An intellectual disability that is characterized by the absence of associated medical and behavioral signs and symptoms.",
                "url": "https://disease-ontology.org/term/DOID:0050889",
                "evidence": [
                    {
                        "id": "0050889",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050889"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0060677",
                "name": "catecholaminergic polymorphic ventricular tachycardia 3",
                "description": "A catecholaminergic polymorphic ventricular tachycardia that is characterized by early onset mortality and has_material_basis_in variation in the chromosomal region 7p22-p14.",
                "url": "https://disease-ontology.org/term/DOID:0060677",
                "evidence": [
                    {
                        "id": "0060677",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060677"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081188",
                "name": "autosomal recessive intellectual developmental disorder 14",
                "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TECR gene on chromosome 19p13.",
                "url": "https://disease-ontology.org/term/DOID:0081188",
                "evidence": [
                    {
                        "id": "0081188",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081188"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum",
                "id": "GO:0005783",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005783",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endomembrane system",
                "id": "GO:0012505",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012505",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "sphingolipid metabolic process",
                "id": "GO:0006665",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006665",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "very long-chain fatty acid biosynthetic process",
                "id": "GO:0042761",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042761",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "very-long-chain enoyl-CoA reductase activity",
                "id": "GO:0102758",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0102758",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZL3",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL3"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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        ],
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                "disease_id": "DOID:3753",
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            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032510",
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            },
            {
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        ],
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                        "id": "Q9VZL5",
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                    }
                ],
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            },
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                "id": "GO:0035658",
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                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/Q9VZL5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "guanyl-nucleotide exchange factor activity",
                "id": "GO:0005085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005085",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "cellular_component": [
            {
                "name": "perinuclear region of cytoplasm",
                "id": "GO:0048471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9VZP9",
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                    }
                ],
                "pmid": ""
            },
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                "name": "lysosomal membrane",
                "id": "GO:0005765",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005765",
                "evidence": [
                    {
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            }
        ],
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    {
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                "name": "Drosophila melanogaster",
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        ],
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        "chemical_mass": 160561.0,
        "gene_names": "MnM;CG14964;CT34810;Dmel\\CG14964;Dmel_CG14964;MnM;dMnM",
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                "disease_id": "DOID:0050646",
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                        "database": "AGR",
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                ],
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                    {
                        "id": "0060654",
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                ],
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            },
            {
                "disease_id": "DOID:0080326",
                "name": "familial hypertrophic cardiomyopathy",
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                "evidence": [
                    {
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                        "url": "https://www.alliancegenome.org/disease/DOID:0080326"
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                ],
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            },
            {
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                "description": "A dilated cardiomyopathy that has_material_basis_in heterozygous mutation in the MYBPC3 gene on chromosome 11p11.",
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                        "id": "0081158",
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                ],
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                ],
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                "url": "https://disease-ontology.org/term/DOID:0081348",
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                ],
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                        "id": "0110310",
                        "database": "AGR",
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            },
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                ],
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                ],
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                ],
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            }
        ],
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            {
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                    {
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                        "id": "Q9VZT8",
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                    }
                ],
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            }
        ],
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                    {
                        "glytoucan_ac": "",
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                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
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                        ],
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                        },
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                    {
                        "glytoucan_ac": "",
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                        "site_category_dict": {
                            "predicted": true
                        },
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                ],
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            }
        ],
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        "protein_name": "Ubiquitin carboxyl-terminal hydrolase",
        "disease": [],
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
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            },
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                    }
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            },
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043161",
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                        "id": "Q9VZU7",
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                    }
                ],
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            },
            {
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                    }
                ],
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                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            },
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                "evidence": [
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of double-strand break repair",
                "id": "GO:2000781",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000781",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "free ubiquitin chain depolymerization",
                "id": "GO:0010995",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010995",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of proteasome assembly",
                "id": "GO:0090364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090364",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "compound eye photoreceptor cell differentiation",
                "id": "GO:0001751",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001751",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9VZU7",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
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                        "id": "Q9VZU7",
                        "url": "https://www.uniprot.org/uniprotkb/Q9VZU7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
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            {
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                "name": "DNA strand elongation involved in mitotic DNA replication",
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        ],
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                "name": "Drosophila melanogaster",
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                        "database": "UniProtKB",
                        "id": "Q9W136",
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                ],
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        ],
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    {
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                ],
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        ],
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            {
                "name": "rescue of stalled ribosome",
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                "name": "ubiquitin protein ligase activity",
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                ],
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                ],
                "pmid": ""
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        ],
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                ],
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                            }
                        ]
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                ]
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                ],
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        ],
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                ],
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        ],
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                "name": "nuclear membrane reassembly",
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                "pmid": ""
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            {
                "name": "autophagosome assembly",
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                "name": "proteasome-mediated ubiquitin-dependent protein catabolic process",
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                "name": "membrane fusion",
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                "pmid": ""
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            {
                "name": "Golgi organization",
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                ],
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        ],
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                ],
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                "name": "cytosol",
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                "disease_id": "DOID:0081175",
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                "url": "https://disease-ontology.org/term/DOID:0081175",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0081175"
                    }
                ],
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            },
            {
                "disease_id": "DOID:9538",
                "name": "multiple myeloma",
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow.",
                "url": "https://disease-ontology.org/term/DOID:9538",
                "evidence": [
                    {
                        "id": "9538",
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                ],
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            {
                "name": "RNA binding",
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                        "id": "Q9W1M9",
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                ],
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        ],
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            {
                "name": "nucleus",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005730",
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                    }
                ],
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                "name": "cytoplasm",
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                    }
                ],
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            },
            {
                "name": "nuclear exosome (RNase complex)",
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                    {
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                        "id": "Q9W1M9",
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                ],
                "pmid": ""
            },
            {
                "name": "nuclear lamina",
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                    {
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                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasmic exosome (RNase complex)",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000177",
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                    {
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                        "id": "Q9W1M9",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "exosome (RNase complex)",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "defense response to virus",
                "id": "GO:0051607",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051607",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "regulation of gene expression",
                "id": "GO:0010468",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010468",
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                ],
                "pmid": ""
            },
            {
                "name": "nuclear-transcribed mRNA catabolic process",
                "id": "GO:0000956",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000956",
                "evidence": [
                    {
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                        "id": "Q9W1M9",
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                ],
                "pmid": ""
            },
            {
                "name": "RNA catabolic process",
                "id": "GO:0006401",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006401",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
                    }
                ],
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            },
            {
                "name": "exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
                "id": "GO:0000467",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000467",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "U4 snRNA 3'-end processing",
                "id": "GO:0034475",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034475",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
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                ],
                "pmid": ""
            },
            {
                "name": "CUT catabolic process",
                "id": "GO:0071034",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear polyadenylation-dependent rRNA catabolic process",
                "id": "GO:0071035",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071035",
                "evidence": [
                    {
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                        "id": "Q9W1M9",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1M9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "TRAMP-dependent tRNA surveillance pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071038",
                "evidence": [
                    {
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                ],
                "pmid": ""
            },
            {
                "name": "poly(A)-dependent snoRNA 3'-end processing",
                "id": "GO:0071051",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071051",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1M9",
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                ],
                "pmid": ""
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        ],
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    {
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                "evidence": [
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                ],
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        ],
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            {
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            {
                "name": "zinc ion binding",
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                    {
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                        "id": "Q9W1P0",
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                ],
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            }
        ],
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            {
                "name": "lysosomal membrane",
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                ],
                "pmid": ""
            },
            {
                "name": "late endosome membrane",
                "id": "GO:0031902",
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                        "id": "Q9W1P0",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "positive regulation of hemocyte proliferation",
                "id": "GO:0035208",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035208",
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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        "protein_name": "",
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    },
    {
        "uniprot_canonical_ac": "Q9W1R1-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "Q9W1R1",
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                ],
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            }
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            {
                "name": "extracellular region",
                "id": "GO:0005576",
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                ],
                "pmid": ""
            }
        ],
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                ],
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        ],
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                    {
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                ],
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        ],
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                "name": "proteasome core complex, beta-subunit complex",
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                "evidence": [
                    {
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                        "id": "Q9W1S5",
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                ],
                "pmid": ""
            },
            {
                "name": "nucleus",
                "id": "GO:0005634",
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                "evidence": [
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                        "id": "Q9W1S5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1S5"
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                ],
                "pmid": ""
            },
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                "name": "cytosol",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                        "id": "Q9W1S5",
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                    }
                ],
                "pmid": ""
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        ],
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            {
                "name": "endopeptidase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004175",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W1S5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1S5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "threonine-type endopeptidase activity",
                "id": "GO:0004298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004298",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "Q9W1S5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1S5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "proteasome-mediated ubiquitin-dependent protein catabolic process",
                "id": "GO:0043161",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043161",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W1S5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1S5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "proteasomal protein catabolic process",
                "id": "GO:0010498",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010498",
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                        "id": "Q9W1S5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1S5"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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                        "id": "Q9W1S9",
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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    {
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                ],
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            }
        ],
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        "protein_name": "",
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            {
                "name": "RNA binding",
                "id": "GO:0003723",
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                        "id": "Q9W1T0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W1T0"
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                ],
                "pmid": ""
            },
            {
                "name": "ubiquitin binding",
                "id": "GO:0043130",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
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            }
        ],
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                "name": "nuclear pore",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005643",
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            }
        ],
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                "name": "RNA export from nucleus",
                "id": "GO:0006405",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006405",
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                ],
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            {
                "name": "transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000972",
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                    }
                ],
                "pmid": ""
            }
        ],
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                ],
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        ],
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                "disease_id": "DOID:0110219",
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                ],
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                "name": "glycerophospholipid metabolic process",
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            {
                "name": "carbohydrate metabolic process",
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                "name": "glycerol-3-phosphate metabolic process",
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                "name": "glycerol-3-phosphate catabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046168",
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            {
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                "name": "sodium ion transport",
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        ],
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            {
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                "name": "post-transcriptional regulation of gene expression",
                "id": "GO:0010608",
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                    }
                ],
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            {
                "name": "sperm individualization",
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                ],
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            {
                "name": "regulation of alternative mRNA splicing, via spliceosome",
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                    {
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                        "id": "Q9W224",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W224"
                    }
                ],
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                        ],
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                            }
                        ]
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        "uniprot_canonical_ac": "Q9W232-1",
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        ],
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                "disease_id": "DOID:0081232",
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                        "id": "0081232",
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            {
                "name": "nucleus",
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                ],
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            },
            {
                "name": "cytoplasm",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W232",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W232"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W232",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W232"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tRNA binding",
                "id": "GO:0000049",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000049",
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                        "database": "UniProtKB",
                        "id": "Q9W232",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "S-adenosylmethionine-dependent methyltransferase activity",
                "id": "GO:0008757",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008757",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W232",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W232"
                    }
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            {
                "name": "tRNA (uridine) methyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016300",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W232",
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                    }
                ],
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            {
                "name": "tRNA (5-carboxymethyluridine(34)-5-O)-methyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0106335",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W232",
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                    }
                ],
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        ],
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                "name": "tRNA wobble uridine modification",
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            {
                "name": "tRNA methylation",
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                "name": "nucleus",
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                "name": "regulation of alternative mRNA splicing, via spliceosome",
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        ],
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                        "id": "Q9W242",
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        "protein_name": "Seminal fluid protein",
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                ],
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            {
                "name": "regulation of microtubule polymerization or depolymerization",
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                ],
                "pmid": ""
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        ],
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    {
        "uniprot_canonical_ac": "Q9W270-1",
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                "disease_id": "DOID:10283",
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                "description": "A male reproductive organ cancer that is located_in the prostate.",
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                ],
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            {
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                "evidence": [
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                        "database": "AGR",
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                ],
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            {
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                "url": "https://disease-ontology.org/term/DOID:12308",
                "evidence": [
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                        "id": "12308",
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                        "url": "https://www.alliancegenome.org/disease/DOID:12308"
                    }
                ],
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            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
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                "evidence": [
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                        "id": "1324",
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                ],
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            {
                "disease_id": "DOID:13580",
                "name": "cholestasis",
                "description": "A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum.",
                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14283",
                "name": "primary hypertrophic osteoarthropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14283",
                "evidence": [
                    {
                        "id": "14283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1520",
                "name": "colon carcinoma",
                "description": "A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:1520",
                "evidence": [
                    {
                        "id": "1520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1520"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2741",
                "name": "bilirubin metabolic disorder",
                "description": "An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.",
                "url": "https://disease-ontology.org/term/DOID:2741",
                "evidence": [
                    {
                        "id": "2741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2998",
                "name": "testicular cancer",
                "description": "A male reproductive system cancer that is located_in the testicles.",
                "url": "https://disease-ontology.org/term/DOID:2998",
                "evidence": [
                    {
                        "id": "2998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3007",
                "name": "breast ductal carcinoma",
                "description": "A breast carcinoma that derives_from the lining of milk ducts.",
                "url": "https://disease-ontology.org/term/DOID:3007",
                "evidence": [
                    {
                        "id": "3007",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3007"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3571",
                "name": "liver cancer",
                "description": "A hepatobiliary system cancer that is located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:3571",
                "evidence": [
                    {
                        "id": "3571",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3571"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9253",
                "name": "gastrointestinal stromal tumor",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9253",
                "evidence": [
                    {
                        "id": "9253",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9253"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9452",
                "name": "steatotic liver disease",
                "description": "A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in at least 5% of hepatocytes.",
                "url": "https://disease-ontology.org/term/DOID:9452",
                "evidence": [
                    {
                        "id": "9452",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9452"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "basolateral plasma membrane",
                "id": "GO:0016323",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016323",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "monoatomic ion transport",
                "id": "GO:0006811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "organic anion transport",
                "id": "GO:0015711",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015711",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium-independent organic anion transport",
                "id": "GO:0043252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "renal tubular secretion",
                "id": "GO:0097254",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097254",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W270",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W270"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9W271-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 684,
        "chemical_mass": 75680.0,
        "gene_names": "Oatp58Da;CG30277;CG3387;Dmel\\CG30277;Dmel_CG30277;Oatp58Da;oatp 58Da",
        "protein_name": "Solute carrier organic anion transporter family member",
        "disease": [
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12236",
                "name": "primary biliary cholangitis",
                "description": "A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts.",
                "url": "https://disease-ontology.org/term/DOID:12236",
                "evidence": [
                    {
                        "id": "12236",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12236"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12308",
                "name": "Dubin-Johnson syndrome",
                "description": "A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin without elevation of liver alanine transaminase and aspartate transaminase enzymes as a result of the deficient ability of hepatocytes to secrete conjugated bilirubin into the bile.",
                "url": "https://disease-ontology.org/term/DOID:12308",
                "evidence": [
                    {
                        "id": "12308",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12308"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1324",
                "name": "lung cancer",
                "description": "A respiratory system cancer that is located_in the lung.",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "id": "1324",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1324"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13580",
                "name": "cholestasis",
                "description": "A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum.",
                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14283",
                "name": "primary hypertrophic osteoarthropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:14283",
                "evidence": [
                    {
                        "id": "14283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1520",
                "name": "colon carcinoma",
                "description": "A colon cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:1520",
                "evidence": [
                    {
                        "id": "1520",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1520"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2741",
                "name": "bilirubin metabolic disorder",
                "description": "An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.",
                "url": "https://disease-ontology.org/term/DOID:2741",
                "evidence": [
                    {
                        "id": "2741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2741"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2998",
                "name": "testicular cancer",
                "description": "A male reproductive system cancer that is located_in the testicles.",
                "url": "https://disease-ontology.org/term/DOID:2998",
                "evidence": [
                    {
                        "id": "2998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3007",
                "name": "breast ductal carcinoma",
                "description": "A breast carcinoma that derives_from the lining of milk ducts.",
                "url": "https://disease-ontology.org/term/DOID:3007",
                "evidence": [
                    {
                        "id": "3007",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3007"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3571",
                "name": "liver cancer",
                "description": "A hepatobiliary system cancer that is located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:3571",
                "evidence": [
                    {
                        "id": "3571",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3571"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9253",
                "name": "gastrointestinal stromal tumor",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9253",
                "evidence": [
                    {
                        "id": "9253",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9253"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9452",
                "name": "steatotic liver disease",
                "description": "A lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in at least 5% of hepatocytes.",
                "url": "https://disease-ontology.org/term/DOID:9452",
                "evidence": [
                    {
                        "id": "9452",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9452"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "basolateral plasma membrane",
                "id": "GO:0016323",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016323",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "monoatomic ion transport",
                "id": "GO:0006811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "organic anion transport",
                "id": "GO:0015711",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015711",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium-independent organic anion transport",
                "id": "GO:0043252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "transmembrane transporter activity",
                "id": "GO:0022857",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022857",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W271",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W271"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9W293-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W293",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W293"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 720,
        "chemical_mass": 81069.0,
        "gene_names": "Plekhm1;CG6613;Dmel\\CG6613;Dmel_CG6613;Plekhm1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110945",
                "name": "autosomal recessive osteopetrosis 6",
                "description": "An osteopetrosis characterized by autosomal recessive inheritance of that has_material_basis_in mutation in the PLEKHM1 gene on chromosome 17q21.31.",
                "url": "https://disease-ontology.org/term/DOID:0110945",
                "evidence": [
                    {
                        "id": "0110945",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110945"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13533",
                "name": "osteopetrosis",
                "description": "An osteosclerosis that has_material_basis_in lack of bone resorption which results_in abnormally hard and brittle bones.",
                "url": "https://disease-ontology.org/term/DOID:13533",
                "evidence": [
                    {
                        "id": "13533",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13533"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W293",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W293"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "small GTPase binding",
                "id": "GO:0031267",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031267",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W293",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W293"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "late endosome",
                "id": "GO:0005770",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005770",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W293",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W293"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "secretory granule-lysosome fusion",
                "id": "GO:0160156",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0160156",
                "evidence": [
                    {
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                ],
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            }
        ],
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                ],
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        ],
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        ],
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        "gene_names": "Acox57D-p;ACox57D-p;Acox57D-p;Acox57Dp;CG9707;D-acox;Dmel\\CG9707;Dmel_CG9707;acox",
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                "url": "https://disease-ontology.org/term/DOID:0111067",
                "evidence": [
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                ],
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            },
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                "evidence": [
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                ],
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                                "id": "40245499",
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                    }
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            },
            {
                "name": "spliceosomal complex",
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                    }
                ],
                "pmid": ""
            },
            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000932",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "Lsm2-8 complex",
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W2P5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "small nuclear ribonucleoprotein complex",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W2P5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "U4/U6 x U5 tri-snRNP complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046540",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W2P5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2P5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sno(s)RNA-containing ribonucleoprotein complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005732",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2P5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2P5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "U6 snRNP",
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                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "tRNA processing",
                "id": "GO:0008033",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "mRNA splicing, via spliceosome",
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                "evidence": [
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "maturation of SSU-rRNA",
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                "evidence": [
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                "name": "Drosophila melanogaster",
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                    }
                ],
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                "glygen_name": "Fruit fly",
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            }
        ],
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        "chemical_mass": 34046.0,
        "gene_names": "CAH14;CAH14;CG15227;Dmel\\CG15227;Dmel_CG15227",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2R0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2R0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2R0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2R0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2R0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2R0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "carbonate dehydratase activity",
                "id": "GO:0004089",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004089",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W2R0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W2R0"
                    }
                ],
                "pmid": ""
            }
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                ],
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                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
                            }
                        ]
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                    {
                        "sequence_org": "G",
                        "sequence_mut": "V",
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                                "database": "UniProtKB",
                                "id": "Q9W369",
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                        "sequence_mut": "A",
                        "comment": "Impairs self-processing. Does not affect homodimerization of the unprocessed form. Loss of carcinine hydrolysis.",
                        "evidence": [
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                                "database": "UniProtKB",
                                "id": "Q9W369",
                                "url": "https://www.uniprot.org/uniprotkb/Q9W369"
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                            {
                                "database": "PubMed",
                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
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                        ]
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                        "sequence_org": "C",
                        "sequence_mut": "S",
                        "comment": "Impairs self-processing.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9W369",
                                "url": "https://www.uniprot.org/uniprotkb/Q9W369"
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                            {
                                "database": "PubMed",
                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
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                        ]
                    },
                    {
                        "sequence_org": "C",
                        "sequence_mut": "W",
                        "comment": "Impairs self-processing.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9W369",
                                "url": "https://www.uniprot.org/uniprotkb/Q9W369"
                            },
                            {
                                "database": "PubMed",
                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
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                "uniprot_canonical_ac": "Q9W369-1",
                "start_pos": "217",
                "end_pos": "217",
                "site_lbl": "Arg217",
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                    {
                        "sequence_org": "R",
                        "sequence_mut": "P",
                        "comment": "In tan1 and tan4; impairs self-processing. Loss of beta-alanyl-dopamine hydrolysis. Lighter pigmentation of the body. In newly emerged female imagoes and fly frass, beta-alanyl-dopamine (NBAD) levels are increased about 3-fold while dopamine levels are reduced by 50 percent. Reduces head histamine contents. Increases carcinine levels. Photoreceptor response to light is abnormal. Electroretinogram (ERG) recordings lack normal 'on' and 'off' transients suggesting an impaired synaptic transmission to postsynaptic cells. Reduces number of synaptic vesicles at the terminal of photoreceptor cells L1-L6.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9W369",
                                "url": "https://www.uniprot.org/uniprotkb/Q9W369"
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                            {
                                "database": "PubMed",
                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
                            },
                            {
                                "database": "PubMed",
                                "id": "16299587",
                                "url": "https://glygen.org/publication/PubMed/16299587"
                            },
                            {
                                "database": "PubMed",
                                "id": "12486147",
                                "url": "https://glygen.org/publication/PubMed/12486147"
                            },
                            {
                                "database": "PubMed",
                                "id": "8580497",
                                "url": "https://glygen.org/publication/PubMed/8580497"
                            },
                            {
                                "database": "PubMed",
                                "id": "5782111",
                                "url": "https://glygen.org/publication/PubMed/5782111"
                            },
                            {
                                "database": "PubMed",
                                "id": "21571070",
                                "url": "https://glygen.org/publication/PubMed/21571070"
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                ]
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            {
                "uniprot_canonical_ac": "Q9W369-1",
                "start_pos": "256",
                "end_pos": "256",
                "site_lbl": "Met256",
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                    {
                        "sequence_org": "M",
                        "sequence_mut": "I",
                        "comment": "In tan5; reduces stability resulting in rapid protein degradation. 4-fold increase in affinity for carcinine. No effect on self-processing.",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "Q9W369",
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                            {
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                                "id": "20439462",
                                "url": "https://glygen.org/publication/PubMed/20439462"
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                ]
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        ],
        "record_id": "batch.fruitfly.9"
    },
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        "uniprot_canonical_ac": "Q9W393-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                        "database": "UniProtKB",
                        "id": "Q9W393",
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                ],
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                "glygen_name": "Fruit fly",
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        "chemical_mass": 27144.0,
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        "protein_name": "Activator of basal transcription 1",
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            {
                "name": "RNA binding",
                "id": "GO:0003723",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003723",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
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                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
                "id": "GO:0000447",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000447",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
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                ],
                "pmid": ""
            },
            {
                "name": "endonucleolytic cleavage to generate mature 5'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
                "id": "GO:0000472",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000472",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)",
                "id": "GO:0000480",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000480",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "small-subunit processome assembly",
                "id": "GO:0034462",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034462",
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                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
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                "pmid": ""
            },
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                "name": "regulation of alternative mRNA splicing, via spliceosome",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000381",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W393",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W393"
                    }
                ],
                "pmid": ""
            }
        ],
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        "record_id": "batch.fruitfly.9"
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    {
        "uniprot_canonical_ac": "Q9W3A7-1",
        "species": [
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                "name": "Drosophila melanogaster",
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                "evidence": [
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                        "id": "Q9W3A7",
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "chemical_mass": 15075.0,
        "gene_names": "Dmel\\CG12661;CG12661;Dmel\\CG12661;Dmel_CG12661",
        "protein_name": "Protein FAM136A",
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        "cellular_component": [
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                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                        "database": "UniProtKB",
                        "id": "Q9W3A7",
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                ],
                "pmid": ""
            }
        ],
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        "uniprot_canonical_ac": "Q9W3C3-1",
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                        "id": "Q9W3C3",
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                ],
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                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "gene_names": "Dmel\\CG2004;CG2004;Dmel\\CG2004;Dmel_CG2004;Dro41-0",
        "protein_name": "CHK kinase-like domain-containing protein",
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            {
                "name": "ecdysteroid 22-kinase activity",
                "id": "GO:0106389",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0106389",
                "evidence": [
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                        "id": "Q9W3F4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3F4"
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                ],
                "common_name": "Fruit fly",
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        ],
        "length": 699,
        "chemical_mass": 75698.0,
        "gene_names": "org-1;CG11202;Dm-ORG-1;Dmel\\CG11202;Dmel_CG11202;Org-1;org-1;org1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060413",
                "name": "chromosome 22q11.2 deletion syndrome, distal",
                "description": "A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 22q11.2 region, distinct from DiGeorge syndrome and velocardiofacial syndrome.",
                "url": "https://disease-ontology.org/term/DOID:0060413",
                "evidence": [
                    {
                        "id": "0060413",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060413"
                    }
                ],
                "weight": 0.0
            },
            {
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                "url": "https://disease-ontology.org/term/DOID:10003",
                "evidence": [
                    {
                        "id": "10003",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10003"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "otitis media",
                "description": "A otitis which involves inflammation of the middle ear.",
                "url": "https://disease-ontology.org/term/DOID:10754",
                "evidence": [
                    {
                        "id": "10754",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10754"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11198",
                "name": "DiGeorge syndrome",
                "description": "A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production.",
                "url": "https://disease-ontology.org/term/DOID:11198",
                "evidence": [
                    {
                        "id": "11198",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11198"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11199",
                "name": "hypoparathyroidism",
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                "url": "https://disease-ontology.org/term/DOID:11199",
                "evidence": [
                    {
                        "id": "11199",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11199"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12583",
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                "url": "https://disease-ontology.org/term/DOID:12583",
                "evidence": [
                    {
                        "id": "12583",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12583"
                    }
                ],
                "weight": 0.0
            },
            {
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                "name": "ventricular septal defect",
                "description": "A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles.",
                "url": "https://disease-ontology.org/term/DOID:1657",
                "evidence": [
                    {
                        "id": "1657",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1657"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1682",
                "name": "congenital heart disease",
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                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
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                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
                    }
                ],
                "weight": 0.0
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                "name": "acute kidney failure",
                "description": "",
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                "evidence": [
                    {
                        "id": "3021",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3021"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6419",
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                "description": "",
                "url": "https://disease-ontology.org/term/DOID:6419",
                "evidence": [
                    {
                        "id": "6419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9408",
                "name": "acute myocardial infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9408",
                "evidence": [
                    {
                        "id": "9408",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9408"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "somatic muscle development",
                "id": "GO:0007525",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007525",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3F4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3F4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell fate specification",
                "id": "GO:0001708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001708",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3F4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3F4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3F4",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3F4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016301",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3R6",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3R6"
                    }
                ],
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            {
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                    {
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                        ],
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                    }
                ]
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        ],
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    {
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                ],
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        ],
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            {
                "name": "transcription coactivator activity",
                "id": "GO:0003713",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003713",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription corepressor activity",
                "id": "GO:0003714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear androgen receptor binding",
                "id": "GO:0050681",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050681",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X0",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X0"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "PML body",
                "id": "GO:0016605",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016605",
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                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X0",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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        ],
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        "chemical_mass": 54518.0,
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            {
                "disease_id": "DOID:0111261",
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                "url": "https://disease-ontology.org/term/DOID:0111261",
                "evidence": [
                    {
                        "id": "0111261",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0111261"
                    }
                ],
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            },
            {
                "disease_id": "DOID:3908",
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                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
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                "evidence": [
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                        "id": "3908",
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                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5138",
                "name": "leiomyomatosis",
                "description": "A leiomyoma that is multiple and diffuse.",
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                "evidence": [
                    {
                        "id": "5138",
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                        "url": "https://www.alliancegenome.org/disease/DOID:5138"
                    }
                ],
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            }
        ],
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            {
                "name": "fumarate hydratase activity",
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                        "id": "Q9W3X5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X5"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "fumarate metabolic process",
                "id": "GO:0006106",
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                        "id": "Q9W3X5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X5"
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                ],
                "pmid": ""
            },
            {
                "name": "tricarboxylic acid cycle",
                "id": "GO:0006099",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006099",
                "evidence": [
                    {
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                        "id": "Q9W3X5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X5"
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                ],
                "pmid": ""
            },
            {
                "name": "malate metabolic process",
                "id": "GO:0006108",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006108",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X5"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W3X5",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W3X5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial matrix",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
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                ],
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            },
            {
                "name": "major mitochondrial derivative",
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                    {
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        ],
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                        ]
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                ]
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                "name": "Drosophila melanogaster",
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                ],
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                "name": "extracellular space",
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                ],
                "pmid": ""
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        ],
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                "name": "proteolysis",
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                "name": "innate immune response",
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                        "id": "Q9W452",
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                    }
                ],
                "pmid": ""
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                        "id": "Q9W482",
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                ],
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        ],
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            {
                "name": "compound eye development",
                "id": "GO:0048749",
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                ],
                "pmid": ""
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            {
                "name": "negative regulation of transcription by RNA polymerase II",
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                ],
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            {
                "name": "positive regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W482",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of DNA-templated transcription",
                "id": "GO:0045892",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045892",
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                        "database": "UniProtKB",
                        "id": "Q9W482",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
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                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of execution phase of apoptosis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1900118",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
                    }
                ],
                "pmid": ""
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        ],
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            {
                "name": "DRM complex",
                "id": "GO:0070176",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070176",
                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
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                ],
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            },
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                "name": "nucleus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                "name": "euchromatin",
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                ],
                "pmid": ""
            },
            {
                "name": "Myb complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031523",
                "evidence": [
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                        "id": "Q9W482",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
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                ],
                "pmid": ""
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            {
                "name": "polytene chromosome",
                "id": "GO:0005700",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005700",
                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W482"
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                ],
                "pmid": ""
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        ],
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                "name": "Drosophila melanogaster",
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                        "id": "Q9W493",
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                ],
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        ],
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            {
                "disease_id": "DOID:0050475",
                "name": "Weill-Marchesani syndrome",
                "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                "url": "https://disease-ontology.org/term/DOID:0050475",
                "evidence": [
                    {
                        "id": "0050475",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
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                ],
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            }
        ],
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            {
                "name": "metalloendopeptidase activity",
                "id": "GO:0004222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W493",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "proteolysis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
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                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix organization",
                "id": "GO:0030198",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030198",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W493",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of epidermal growth factor receptor signaling pathway",
                "id": "GO:0042059",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042059",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W493",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of imaginal disc-derived wing vein specification",
                "id": "GO:0110109",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0110109",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9W493",
                        "url": "https://www.uniprot.org/uniprotkb/Q9W493"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
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                ],
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                ],
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        "cellular_component": [
            {
                "name": "mitochondrial matrix",
                "id": "GO:0005759",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005759",
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                "name": "fatty acid biosynthetic process",
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            {
                "name": "estradiol 17-beta-dehydrogenase [NAD(P)+] activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004303",
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                "name": "oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor",
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                ],
                "pmid": ""
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            {
                "name": "3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity",
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                        "database": "UniProtKB",
                        "id": "Q9XZ19",
                        "url": "https://www.uniprot.org/uniprotkb/Q9XZ19"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9XZ19",
                        "url": "https://www.uniprot.org/uniprotkb/Q9XZ19"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Cdc73/Paf1 complex",
                "id": "GO:0016593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9XZ19",
                        "url": "https://www.uniprot.org/uniprotkb/Q9XZ19"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "Q9Y1T2-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 1067,
        "chemical_mass": 116704.0,
        "gene_names": "Apc2;APC2;APC;Apc2;CG6193;D-APC2;Dm APC2;Dmel\\CG6193;Dmel_CG6193;E-APC dAPC2;E-APC;apc2;d-APC2;dAPC2/E-APC;dAPC2;dApc2;dapc2;e-apc",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050424",
                "name": "familial adenomatous polyposis",
                "description": "An intestinal disease that is characterized by predisposition to colon cancer.",
                "url": "https://disease-ontology.org/term/DOID:0050424",
                "evidence": [
                    {
                        "id": "0050424",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050424"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
                    {
                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050902",
                "name": "medulloblastoma",
                "description": "An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor.",
                "url": "https://disease-ontology.org/term/DOID:0050902",
                "evidence": [
                    {
                        "id": "0050902",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050902"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0061143",
                "name": "complex cortical dysplasia with other brain malformations 10",
                "description": "A complex cortical dysplasia with other brain malformations characterized by severely impaired global development associated with abnormalities on brain imaging, including lissencephaly, cortical dysplasia, subcortical heterotopia, and paucity of white matter that has_material_basis_in homozygous or compound heterozygous mutation in the APC2 gene on chromosome 19p13.",
                "url": "https://disease-ontology.org/term/DOID:0061143",
                "evidence": [
                    {
                        "id": "0061143",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061143"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080409",
                "name": "familial adenomatous polyposis 1",
                "description": "A familial adenomatous polyposis that is characterized by predisposition to cancer and that has_material_basis_in heterozygous mutation in the APC gene on chromosome 5q22. Affected individuals usually develop hundreds to thousands of adenomatous polyps of the colon and rectum, a small proportion of which will progress to colorectal carcinoma if not surgically treated.",
                "url": "https://disease-ontology.org/term/DOID:0080409",
                "evidence": [
                    {
                        "id": "0080409",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080409"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081218",
                "name": "autosomal recessive intellectual developmental disorder 74",
                "description": "An autosomal recessive intellectual developmental disorder that is characterized by intellectual impairment, macrocephaly, and dysmorphic features and that has_material_basis_in homozygous mutation in the APC2 gene on chromosome 19p13. Epilepsy with eyelid myoclonus has also been reported.",
                "url": "https://disease-ontology.org/term/DOID:0081218",
                "evidence": [
                    {
                        "id": "0081218",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081218"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111349",
                "name": "hereditary desmoid disease",
                "description": "A syndrome characterized by extraintestinal manifestation of familial adenomatous polyposis that has_material_basis_in in some cases by extreme 3' mutation in APC on 5q22.2.",
                "url": "https://disease-ontology.org/term/DOID:0111349",
                "evidence": [
                    {
                        "id": "0111349",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111349"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0112104",
                "name": "Sotos syndrome 3",
                "description": "A Sotos syndrome that has_material_basis_in homozygous mutation in the APC2 gene on chromosome 19p13.3.",
                "url": "https://disease-ontology.org/term/DOID:0112104",
                "evidence": [
                    {
                        "id": "0112104",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112104"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10283",
                "name": "prostate cancer",
                "description": "A male reproductive organ cancer that is located_in the prostate.",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "id": "10283",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10283"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1380",
                "name": "endometrial cancer",
                "description": "A uterine cancer that is located_in tissues lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:1380",
                "evidence": [
                    {
                        "id": "1380",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1380"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:234",
                "name": "colon adenocarcinoma",
                "description": "A colon carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:234",
                "evidence": [
                    {
                        "id": "234",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:234"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2394",
                "name": "ovarian cancer",
                "description": "A female reproductive organ cancer that is located_in the ovary.",
                "url": "https://disease-ontology.org/term/DOID:2394",
                "evidence": [
                    {
                        "id": "2394",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2394"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2671",
                "name": "transitional cell carcinoma",
                "description": "A carcinoma that derives_from transitional epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:2671",
                "evidence": [
                    {
                        "id": "2671",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2671"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2871",
                "name": "endometrial carcinoma",
                "description": "A endometrial cancer that is located_in the tissue lining the uterus.",
                "url": "https://disease-ontology.org/term/DOID:2871",
                "evidence": [
                    {
                        "id": "2871",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2871"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:299",
                "name": "adenocarcinoma",
                "description": "A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue.",
                "url": "https://disease-ontology.org/term/DOID:299",
                "evidence": [
                    {
                        "id": "299",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:299"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3025",
                "name": "acinar cell carcinoma",
                "description": "A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from spindle cells and/or derives_from giant cells.",
                "url": "https://disease-ontology.org/term/DOID:3025",
                "evidence": [
                    {
                        "id": "3025",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3025"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3121",
                "name": "gallbladder cancer",
                "description": "A biliary tract cancer that is located_in the gallbladder.",
                "url": "https://disease-ontology.org/term/DOID:3121",
                "evidence": [
                    {
                        "id": "3121",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3121"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4450",
                "name": "renal cell carcinoma",
                "description": "A renal carcinoma that has_material_basis_in the lining of the proximal convoluted renal tubule of the kidney.",
                "url": "https://disease-ontology.org/term/DOID:4450",
                "evidence": [
                    {
                        "id": "4450",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4450"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4947",
                "name": "cholangiocarcinoma",
                "description": "A bile duct adenocarcinoma that has_material_basis_in bile duct epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:4947",
                "evidence": [
                    {
                        "id": "4947",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4947"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:657",
                "name": "adenoma",
                "description": "A cell type benign neoplasm that is composed_of epithelial tissue in which tumor cells form glands or glandlike structures.",
                "url": "https://disease-ontology.org/term/DOID:657",
                "evidence": [
                    {
                        "id": "657",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:657"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "basal cortex",
                "id": "GO:0045180",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045180",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical cortex",
                "id": "GO:0045179",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045179",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell cortex",
                "id": "GO:0005938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005938",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dendrite",
                "id": "GO:0030425",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030425",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuronal cell body",
                "id": "GO:0043025",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cleavage furrow",
                "id": "GO:0032154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "catenin complex",
                "id": "GO:0016342",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016342",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "beta-catenin destruction complex",
                "id": "GO:0030877",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030877",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-containing complex",
                "id": "GO:0032991",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032991",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell periphery",
                "id": "GO:0071944",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071944",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell fate specification",
                "id": "GO:0001708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001708",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell migration",
                "id": "GO:0016477",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016477",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of canonical Wnt signaling pathway",
                "id": "GO:0090090",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090090",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
                        "url": "https://www.uniprot.org/uniprotkb/Q9Y1T2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "brain development",
                "id": "GO:0007420",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007420",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9Y1T2",
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                "name": "extracellular region",
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                    }
                ],
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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                ],
                "pmid": ""
            }
        ],
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    {
        "uniprot_canonical_ac": "A0A0B4LHE9-1",
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                ],
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        ],
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                ],
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            }
        ],
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        "chemical_mass": 34058.0,
        "gene_names": "Dmel\\CG46434;CG46434;Dmel_CG46434",
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    },
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        "uniprot_canonical_ac": "A0AQH0-1",
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                ],
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        ],
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        "protein_name": "Proteasome subunit beta",
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                "url": "https://disease-ontology.org/term/DOID:0080199",
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                    }
                ],
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                "url": "https://disease-ontology.org/term/DOID:11394",
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                "description": "A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.",
                "url": "https://disease-ontology.org/term/DOID:12858",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12858"
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            },
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                "disease_id": "DOID:13976",
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                        "database": "AGR",
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                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
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            },
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                        "url": "https://www.alliancegenome.org/disease/DOID:3748"
                    }
                ],
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                ],
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                "url": "https://disease-ontology.org/term/DOID:7147",
                "evidence": [
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                        "id": "7147",
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                        "url": "https://www.alliancegenome.org/disease/DOID:7147"
                    }
                ],
                "weight": 0.0
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                        "id": "7188",
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                        "url": "https://www.alliancegenome.org/disease/DOID:7188"
                    }
                ],
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                "url": "https://disease-ontology.org/term/DOID:8161",
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                        "id": "8161",
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                ],
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                    }
                ],
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            },
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                        "id": "A0AQH0",
                        "url": "https://www.uniprot.org/uniprotkb/A0AQH0"
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                ],
                "pmid": ""
            }
        ],
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                    {
                        "database": "UniProtKB",
                        "id": "A0AQH0",
                        "url": "https://www.uniprot.org/uniprotkb/A0AQH0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "threonine-type endopeptidase activity",
                "id": "GO:0004298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004298",
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                        "database": "UniProtKB",
                        "id": "A0AQH0",
                        "url": "https://www.uniprot.org/uniprotkb/A0AQH0"
                    }
                ],
                "pmid": ""
            }
        ],
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                "name": "proteasome-mediated ubiquitin-dependent protein catabolic process",
                "id": "GO:0043161",
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                    {
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                        "id": "A0AQH0",
                        "url": "https://www.uniprot.org/uniprotkb/A0AQH0"
                    }
                ],
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            },
            {
                "name": "proteasomal protein catabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010498",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0AQH0",
                        "url": "https://www.uniprot.org/uniprotkb/A0AQH0"
                    }
                ],
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                "uniprot_canonical_ac": "A0AQH0-1",
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                "end_pos": "217",
                "site_lbl": "Thr217",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
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                "name": "CP2 mannose-ethanolamine phosphotransferase activity",
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            {
                "disease_id": "DOID:0050854",
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                "url": "https://disease-ontology.org/term/DOID:0050854",
                "evidence": [
                    {
                        "id": "0050854",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050854"
                    }
                ],
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            {
                "disease_id": "DOID:0080270",
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                "url": "https://disease-ontology.org/term/DOID:0080270",
                "evidence": [
                    {
                        "id": "0080270",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080270"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0090029",
                "name": "CINCA Syndrome",
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                "url": "https://disease-ontology.org/term/DOID:0090029",
                "evidence": [
                    {
                        "id": "0090029",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090029"
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                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0090062",
                "evidence": [
                    {
                        "id": "0090062",
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                    }
                ],
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            },
            {
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                "url": "https://disease-ontology.org/term/DOID:0090063",
                "evidence": [
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                        "url": "https://www.alliancegenome.org/disease/DOID:0090063"
                    }
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                "url": "https://disease-ontology.org/term/DOID:12306",
                "evidence": [
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                        "id": "12306",
                        "database": "AGR",
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                    }
                ],
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            },
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                    {
                        "id": "1555",
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                ],
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                    }
                ],
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            },
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                "evidence": [
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                    {
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                ],
                "pmid": ""
            }
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    },
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            {
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            }
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                "evidence": [
                    {
                        "id": "0050629",
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            }
        ],
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            {
                "name": "7-methylguanosine cap hypermethylation",
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            },
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                    }
                ],
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            },
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                "pmid": ""
            },
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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                    {
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                    }
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                "pmid": ""
            },
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                    }
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                "pmid": ""
            },
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                    }
                ],
                "pmid": ""
            },
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                    }
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                "pmid": ""
            }
        ],
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            {
                "name": "U7 snRNA binding",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
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                    }
                ],
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            }
        ],
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        "protein_name": "PRA1 family protein",
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            {
                "name": "Golgi apparatus",
                "id": "GO:0005794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z823",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
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                    {
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                        "id": "A1Z823",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic vesicle",
                "id": "GO:0008021",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008021",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
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                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "A1Z863-1",
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                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
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                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Csgalnact;CG12913;Csgalnact;Dmel\\CG12913;Dmel_CG12913;dCSGalNAcT1",
        "protein_name": "Hexosyltransferase",
        "disease": [],
        "cellular_component": [
            {
                "name": "Golgi membrane",
                "id": "GO:0000139",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000139",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            },
            {
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005794",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Golgi cisterna membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032580",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "wound healing",
                "id": "GO:0042060",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042060",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chondroitin sulfate proteoglycan biosynthetic process",
                "id": "GO:0050650",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050650",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase activity",
                "id": "GO:0047237",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047237",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity",
                "id": "GO:0047238",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0047238",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z863",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z863"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1Z882-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z882",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z882"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 593,
        "chemical_mass": 68220.0,
        "gene_names": "Ir47a;47a;CG12900;DmelIR47a;Dmel\\CG12900;Dmel_CG12900;IR47a;Ir47a",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "detection of chemical stimulus",
                "id": "GO:0009593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009593",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z882",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z882"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z882",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z882"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z882",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z882"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ligand-gated monoatomic ion channel activity",
                "id": "GO:0015276",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015276",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z882",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z882"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1Z8H4-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8H4",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8H4"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 131,
        "chemical_mass": 14183.0,
        "gene_names": "Cpr47Ec;CG9077;Cpr47Ec;Cpr47eg;DmelCpr47Ec;Dmel\\CG9077;Dmel_CG9077",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "structural constituent of chitin-based larval cuticle",
                "id": "GO:0008010",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008010",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8H4",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8H4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8H4",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8H4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "chitin-based extracellular matrix",
                "id": "GO:0062129",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0062129",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8H4",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8H4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1Z8I5-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8I5",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8I5"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 94,
        "chemical_mass": 10654.0,
        "gene_names": "CG13212;CG13212;CG18336;Dmel\\CG18336;Dmel_CG18336",
        "protein_name": "Ciliary microtubule inner protein 2A-C-like domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "microtubule cytoskeleton",
                "id": "GO:0015630",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015630",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8I5",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8I5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axoneme",
                "id": "GO:0005930",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005930",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z8I5",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z8I5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A1Z8T9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
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                        "id": "A1Z8T9",
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            {
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                ],
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        ],
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            {
                "name": "structural constituent of chitin-based larval cuticle",
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                ],
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        ],
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                ],
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                    {
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                ],
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            }
        ],
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        ],
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        ],
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                "name": "intracellular iron ion homeostasis",
                "id": "GO:0006879",
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                "pmid": ""
            },
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                "name": "2 iron, 2 sulfur cluster binding",
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                "pmid": ""
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            {
                "name": "iron-sulfur cluster binding",
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        ],
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            {
                "name": "DRM complex",
                "id": "GO:0070176",
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                ],
                "pmid": ""
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                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
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                "evidence": [
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                ],
                "pmid": ""
            }
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                "name": "negative regulation of transcription by RNA polymerase II",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "spermatogenesis",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007283",
                "evidence": [
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                "pmid": ""
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            {
                "name": "protein-containing complex binding",
                "id": "GO:0044877",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044877",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z949",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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                ],
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            {
                "name": "nucleus",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "nucleolus",
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                ],
                "pmid": ""
            },
            {
                "name": "Cdc73/Paf1 complex",
                "id": "GO:0016593",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016593",
                "evidence": [
                    {
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                        "id": "A1Z9G9",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "transcription elongation by RNA polymerase II",
                "id": "GO:0006368",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006368",
                "evidence": [
                    {
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                        "id": "A1Z9G9",
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                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of transcription elongation by RNA polymerase II",
                "id": "GO:0032968",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032968",
                "evidence": [
                    {
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                        "id": "A1Z9G9",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "RNA polymerase II complex binding",
                "id": "GO:0000993",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000993",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1Z9G9",
                        "url": "https://www.uniprot.org/uniprotkb/A1Z9G9"
                    }
                ],
                "pmid": ""
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        ],
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    {
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        ],
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            {
                "name": "membrane",
                "id": "GO:0016020",
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                "evidence": [
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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    {
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                ],
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            },
            {
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                ],
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            {
                "disease_id": "DOID:0110399",
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                ],
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                        "id": "A1ZA01",
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            {
                "name": "zinc ion binding",
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                ],
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            },
            {
                "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZA01"
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                ],
                "pmid": ""
            },
            {
                "name": "heme binding",
                "id": "GO:0020037",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0020037",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A1ZA01",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZA01"
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                ],
                "pmid": ""
            },
            {
                "name": "nuclear receptor activity",
                "id": "GO:0004879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004879",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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                ],
                "pmid": ""
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            {
                "name": "DNA-templated transcription",
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            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
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                ],
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            },
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                "name": "neuron remodeling",
                "id": "GO:0016322",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016322",
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                ],
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            {
                "name": "positive regulation of transcription by RNA polymerase II",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944",
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                        "id": "A1ZA01",
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                ],
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            },
            {
                "name": "neuron differentiation",
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                "evidence": [
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                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZA01"
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                ],
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            },
            {
                "name": "regulation of circadian rhythm",
                "id": "GO:0042752",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042752",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZA01"
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                ],
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            {
                "name": "regulation of gene expression",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010468",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZA01",
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                ],
                "pmid": ""
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            {
                "name": "locomotor rhythm",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045475",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A1ZA01",
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                ],
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            },
            {
                "name": "axon guidance",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A1ZA01",
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                ],
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            {
                "name": "positive regulation of axon extension involved in axon guidance",
                "id": "GO:0048842",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048842",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZA01"
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                ],
                "pmid": ""
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            {
                "name": "mushroom body development",
                "id": "GO:0016319",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016319",
                "evidence": [
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                        "id": "A1ZA01",
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                ],
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            {
                "name": "imaginal disc-derived wing expansion",
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                "evidence": [
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                ],
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        ],
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                "disease_id": "DOID:0050649",
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                "description": "A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin (TF) on chromosome 3q22.",
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                "name": "iron ion binding",
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                "name": "extracellular space",
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                    }
                ],
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            },
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                "name": "early endosome",
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                    {
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                        "id": "A1ZAC0",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAC0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
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                ],
                "pmid": ""
            },
            {
                "name": "recycling endosome",
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                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "iron ion transport",
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                "pmid": ""
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    {
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            {
                "name": "extracellular space",
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                "pmid": ""
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                "name": "response to wounding",
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                ],
                "pmid": ""
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            {
                "name": "phospholipase C-activating G protein-coupled receptor signaling pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007200",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
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            {
                "name": "positive regulation of homotypic cell-cell adhesion",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                "pmid": ""
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            {
                "name": "cellular response to amino acid stimulus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071230",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                "pmid": ""
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            {
                "name": "positive regulation of multicellular organism growth",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
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            {
                "name": "positive regulation of peptide hormone secretion",
                "id": "GO:0090277",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090277",
                "evidence": [
                    {
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                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
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            {
                "name": "negative regulation of growth",
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                "evidence": [
                    {
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                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
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            {
                "name": "positive regulation of humoral immune response",
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                    {
                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of antimicrobial peptide production",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
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        ],
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            {
                "name": "cytokine activity",
                "id": "GO:0005125",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005125",
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                        "database": "UniProtKB",
                        "id": "A1ZAQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZAQ9"
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                ],
                "pmid": ""
            }
        ],
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    {
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                        "id": "A1ZB23",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZB23"
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                ],
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        ],
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    {
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                "name": "Drosophila melanogaster",
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                        "id": "A1ZB58",
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                ],
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    {
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                ],
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        ],
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            {
                "name": "glutathione transferase activity",
                "id": "GO:0004364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004364",
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                        "id": "A1ZB68",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZB68"
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                ],
                "pmid": ""
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        ],
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                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "glutathione metabolic process",
                "id": "GO:0006749",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006749",
                "evidence": [
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                        "id": "A1ZB68",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZB68"
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                ],
                "pmid": ""
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        ],
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    {
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                ],
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        ],
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        "gene_names": "DptB;147473_at;BcDNA:RH29451;CG10794;DiptB;Diptericin;Dipt;Dmel\\CG10794;Dmel_CG10794;DptB;Dpt;diptB;dpt B;dptB;dptlp",
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            {
                "name": "extracellular space",
                "id": "GO:0005615",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZBF6"
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                ],
                "pmid": ""
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        ],
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            {
                "name": "innate immune response",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045087",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBF6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBF6"
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                ],
                "pmid": ""
            },
            {
                "name": "defense response to Gram-positive bacterium",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050830",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBF6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBF6"
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                ],
                "pmid": ""
            },
            {
                "name": "response to wounding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009611",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZBF6"
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                ],
                "pmid": ""
            },
            {
                "name": "humoral immune response",
                "id": "GO:0006959",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006959",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBF6",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBF6"
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                ],
                "pmid": ""
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        ],
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    {
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        ],
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            {
                "disease_id": "DOID:0080155",
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                "url": "https://disease-ontology.org/term/DOID:0080155",
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                ],
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            },
            {
                "disease_id": "DOID:0080208",
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                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
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                "evidence": [
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                        "id": "10652",
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                "name": "long-chain fatty acyl-CoA dehydrogenase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004466",
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                    {
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                        "id": "A1ZBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                ],
                "pmid": ""
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            {
                "name": "flavin adenine dinucleotide binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050660",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                "pmid": ""
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            {
                "name": "fatty-acyl-CoA binding",
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                "evidence": [
                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                ],
                "pmid": ""
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            {
                "name": "very-long-chain fatty acyl-CoA dehydrogenase activity",
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                        "database": "UniProtKB",
                        "id": "A1ZBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                ],
                "pmid": ""
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        ],
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                "name": "mitochondrion",
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                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                "pmid": ""
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            {
                "name": "mitochondrial inner membrane",
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                        "id": "A1ZBJ2",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBJ2"
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                ],
                "pmid": ""
            }
        ],
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                "name": "fatty acid beta-oxidation using acyl-CoA dehydrogenase",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033539",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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                ],
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        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "insemination",
                "id": "GO:0007320",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007320",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBQ4",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBQ4"
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                ],
                "pmid": ""
            },
            {
                "name": "sensory perception of smell",
                "id": "GO:0007608",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007608",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBQ4",
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                ],
                "pmid": ""
            },
            {
                "name": "sensory perception of chemical stimulus",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007606",
                "evidence": [
                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
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                    {
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                        "id": "A1ZBQ4",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular space",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "odorant binding",
                "id": "GO:0005549",
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                    }
                ],
                "pmid": ""
            }
        ],
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    {
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            {
                "name": "Drosophila melanogaster",
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                    {
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                        "id": "A1ZBY3",
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                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
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        ],
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        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "neuron projection membrane",
                "id": "GO:0032589",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032589",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY3",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
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                "evidence": [
                    {
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                        "id": "A1ZBY3",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY3",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "synapse organization",
                "id": "GO:0050808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY3",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "salt aversion",
                "id": "GO:0035199",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035199",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY3",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sensory perception of salty taste",
                "id": "GO:0050914",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050914",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A1ZBY3",
                        "url": "https://www.uniprot.org/uniprotkb/A1ZBY3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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            {
                "uniprot_canonical_ac": "A1ZBY3-1",
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                "site_lbl": "Thr37",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 37,
                        "start_aa": "Thr",
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                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr37",
                        "evidence": [
                            {
                                "id": "GLY_001163",
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                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A8DY49-1",
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            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DY49",
                        "url": "https://www.uniprot.org/uniprotkb/A8DY49"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 104,
        "chemical_mass": 11193.0,
        "gene_names": "Dmel\\CG34215;CG34215;Dmel\\CG34215;Dmel_CG34215",
        "protein_name": "Single domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DY49",
                        "url": "https://www.uniprot.org/uniprotkb/A8DY49"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYD7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYD7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYD7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 295,
        "chemical_mass": 34038.0,
        "gene_names": "Dmel\\CG34444;CG30070;CG34444;Dmel\\CG34444;Dmel_CG34444",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYF7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 346,
        "chemical_mass": 38737.0,
        "gene_names": "mrj;CG8448;Dmel\\CG8448;Dmel_CG8448;MRJ;dMRJ;dmrj;mrjA;mrj",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110305",
                "name": "autosomal dominant limb-girdle muscular dystrophy type 1",
                "description": "An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the DNAJB6 gene on chromosome 7q36.",
                "url": "https://disease-ontology.org/term/DOID:0110305",
                "evidence": [
                    {
                        "id": "0110305",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110305"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111214",
                "name": "autosomal recessive distal hereditary motor neuronopathy 5",
                "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by young adult onset of slowly progressive distal muscle weakness and atrophy resulting in gait impairment and loss of reflexes that has_material_basis_in homozygous or compound heterozygous mutation in DNAJB2 on 2q35.",
                "url": "https://disease-ontology.org/term/DOID:0111214",
                "evidence": [
                    {
                        "id": "0111214",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111214"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "unfolded protein binding",
                "id": "GO:0051082",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051082",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-folding chaperone binding",
                "id": "GO:0051087",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051087",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein folding chaperone",
                "id": "GO:0044183",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044183",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein folding",
                "id": "GO:0006457",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006457",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYF7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYF7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYH6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYH6",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYH6"
                    }
                ],
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                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
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        "gene_names": "Dmel\\CG34194;CG34194;Dmel\\CG34194;Dmel_CG34194",
        "protein_name": "Serine palmitoyltransferase small subunit B",
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            {
                "disease_id": "DOID:0070459",
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                "url": "https://disease-ontology.org/term/DOID:0070459",
                "evidence": [
                    {
                        "id": "0070459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070460",
                "name": "hereditary spastic paraplegia 90B",
                "description": "A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous mutation in the SPTSSA gene on chromosome 14q13.1.",
                "url": "https://disease-ontology.org/term/DOID:0070460",
                "evidence": [
                    {
                        "id": "0070460",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070460"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "serine palmitoyltransferase complex",
                "id": "GO:0017059",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0017059",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYH6",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYH6",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYH6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "sphingolipid metabolic process",
                "id": "GO:0006665",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006665",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYH6",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "A8DYL2-1",
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            {
                "name": "Drosophila melanogaster",
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                    {
                        "database": "UniProtKB",
                        "id": "A8DYL2",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYL2"
                    }
                ],
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                "glygen_name": "Fruit fly",
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        ],
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        "disease": [],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYL2",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYT7-1",
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            {
                "name": "Drosophila melanogaster",
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                ],
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        ],
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        "gene_names": "CG9966;CG31684;CG34448;CG9966;Dmel\\CG34448;Dmel_CG34448",
        "protein_name": "Lipase domain-containing protein",
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            {
                "disease_id": "DOID:0080000",
                "name": "muscular disease",
                "description": "A musculoskeletal system disease that affects the muscles.",
                "url": "https://disease-ontology.org/term/DOID:0080000",
                "evidence": [
                    {
                        "id": "0080000",
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
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                "evidence": [
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                ],
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            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
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                    {
                        "id": "10763",
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                ],
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            },
            {
                "disease_id": "DOID:1168",
                "name": "familial hyperlipidemia",
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                "evidence": [
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                        "database": "AGR",
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11801",
                "name": "protein-energy malnutrition",
                "description": "A nutritional deficiency disease that is characterized by inadequate dietary protein and calories, which can have profound systemic effects including decreased metabolism, altered tissue distribution, compromised immunity, and impaired growth, and has_material_basis_in dietary deprivation.",
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                "evidence": [
                    {
                        "id": "11801",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11801"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1184",
                "name": "nephrotic syndrome",
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                "url": "https://disease-ontology.org/term/DOID:1184",
                "evidence": [
                    {
                        "id": "1184",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1184"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1287",
                "name": "cardiovascular system disease",
                "description": "A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.",
                "url": "https://disease-ontology.org/term/DOID:1287",
                "evidence": [
                    {
                        "id": "1287",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1287"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1312",
                "name": "focal segmental glomerulosclerosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1312",
                "evidence": [
                    {
                        "id": "1312",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1312"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13809",
                "name": "familial combined hyperlipidemia",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:13809",
                "evidence": [
                    {
                        "id": "13809",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13809"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14118",
                "name": "familial lipoprotein lipase deficiency",
                "description": "A familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides.",
                "url": "https://disease-ontology.org/term/DOID:14118",
                "evidence": [
                    {
                        "id": "14118",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14118"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
                    {
                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2018",
                "name": "hyperinsulinism",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2018",
                "evidence": [
                    {
                        "id": "2018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2237",
                "name": "hepatitis",
                "description": "A liver disease that is characterized as an inflammation of the liver.",
                "url": "https://disease-ontology.org/term/DOID:2237",
                "evidence": [
                    {
                        "id": "2237",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2237"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:326",
                "name": "ischemia",
                "description": "A vascular disease that is characterized by a restriction in blood supply to tissues.",
                "url": "https://disease-ontology.org/term/DOID:326",
                "evidence": [
                    {
                        "id": "326",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:326"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:341",
                "name": "peripheral vascular disease",
                "description": "A vascular disease that is characterized by obstruction of vessels not within the coronary, aortic arch vasculature, or brain.",
                "url": "https://disease-ontology.org/term/DOID:341",
                "evidence": [
                    {
                        "id": "341",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:341"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3526",
                "name": "cerebral infarction",
                "description": "A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain.",
                "url": "https://disease-ontology.org/term/DOID:3526",
                "evidence": [
                    {
                        "id": "3526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3526"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:557",
                "name": "kidney disease",
                "description": "A urinary system disease that is located_in the kidney.",
                "url": "https://disease-ontology.org/term/DOID:557",
                "evidence": [
                    {
                        "id": "557",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:557"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9744",
                "name": "type 1 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by destruction of pancreatic beta cells resulting in absent or extremely low insulin production.",
                "url": "https://disease-ontology.org/term/DOID:9744",
                "evidence": [
                    {
                        "id": "9744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9970",
                "name": "obesity",
                "description": "An overnutrition that is characterized by excess body fat, traditionally defined as an elevated ratio of weight to height (specifically 30 kilograms per meter squared), has_material_basis_in a multifactorial etiology related to excess nutrition intake, decreased caloric utilization, and genetic susceptibility, and possibly medications and certain disorders of metabolism, endocrine function, and mental illness.",
                "url": "https://disease-ontology.org/term/DOID:9970",
                "evidence": [
                    {
                        "id": "9970",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9970"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYT7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYT7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "lipid metabolic process",
                "id": "GO:0006629",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006629",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYT7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYT7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lipid catabolic process",
                "id": "GO:0016042",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016042",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYT7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYT7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "lipase activity",
                "id": "GO:0016298",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016298",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYT7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYT7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "triacylglycerol lipase activity",
                "id": "GO:0004806",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004806",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYT7",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYT7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYV1-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYV1",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYV1"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 112,
        "chemical_mass": 12916.0,
        "gene_names": "Dmel\\CG34178;CG34178;Dmel\\CG34178;Dmel_CG34178",
        "protein_name": "Single domain-containing protein",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYV1",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYV1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8DYV9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8DYV9",
                        "url": "https://www.uniprot.org/uniprotkb/A8DYV9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 76,
        "chemical_mass": 8391.0,
        "gene_names": "Dmel\\CG34180;CG34180;Dmel\\CG34180;Dmel_CG34180",
        "protein_name": "Secreted protein",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8JTM7-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 4769,
        "chemical_mass": 530166.0,
        "gene_names": "mgl;CG12139;CG12654;CG15316;CG34339;CG34352;CG42611;CT7830;Dm CG34352;Dmel\\CG42611;Dmel_CG42611;LDLR;LRP-2;Megalin;Mgl;SOSIE;anon-WO0140519.108;lrp2;megalin;mgl",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0090144",
                "name": "Donnai-Barrow syndrome",
                "description": "A syndrome that is characterized by facial and ocular abnormalities, sensorineural hearing loss, agenesis of the corpus callosum, variable intellectual disability, and proteinuria that has_material_basis_in homozygous or compound heterozygous mutation in the LDL receptor related protein 2 gene (LRP2) on chromosome 2q31.",
                "url": "https://disease-ontology.org/term/DOID:0090144",
                "evidence": [
                    {
                        "id": "0090144",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1062",
                "name": "Fanconi syndrome",
                "description": "A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.",
                "url": "https://disease-ontology.org/term/DOID:1062",
                "evidence": [
                    {
                        "id": "1062",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1062"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10976",
                "name": "membranous glomerulonephritis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10976",
                "evidence": [
                    {
                        "id": "10976",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10976"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11829",
                "name": "degenerative myopia",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11829",
                "evidence": [
                    {
                        "id": "11829",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11829"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11830",
                "name": "myopia",
                "description": "A refractive error characterized by the inability to see farther objects clearly.",
                "url": "https://disease-ontology.org/term/DOID:11830",
                "evidence": [
                    {
                        "id": "11830",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11830"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1682",
                "name": "congenital heart disease",
                "description": "A physical disorder that is characterized by problems with the heart's structure that are present at birth.",
                "url": "https://disease-ontology.org/term/DOID:1682",
                "evidence": [
                    {
                        "id": "1682",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1682"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2527",
                "name": "nephrosis",
                "description": "A proteinuria that is characterized by the leaking of blood protein into the urine, swelling or edema, and degenerative lesions without inflammation.",
                "url": "https://disease-ontology.org/term/DOID:2527",
                "evidence": [
                    {
                        "id": "2527",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2527"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7188",
                "name": "autoimmune thyroiditis",
                "description": "An autoimmune disease of endocrine system that involves inflammation located_in thyroid gland caused by the immune system reacting against its own tissues.",
                "url": "https://disease-ontology.org/term/DOID:7188",
                "evidence": [
                    {
                        "id": "7188",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7188"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:783",
                "name": "end stage renal disease",
                "description": "A chronic kidney disease is characterized by non-functioning kidneys, as the final stage in chronic kidney disease.",
                "url": "https://disease-ontology.org/term/DOID:783",
                "evidence": [
                    {
                        "id": "783",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:783"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:898",
                "name": "autosomal dominant polycystic kidney disease",
                "description": "A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal dominant fashion.",
                "url": "https://disease-ontology.org/term/DOID:898",
                "evidence": [
                    {
                        "id": "898",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:898"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "clathrin-coated pit",
                "id": "GO:0005905",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005905",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "receptor complex",
                "id": "GO:0043235",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043235",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of endocytosis",
                "id": "GO:0030100",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030100",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "receptor-mediated endocytosis",
                "id": "GO:0006898",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006898",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chitin-based cuticle development",
                "id": "GO:0040003",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0040003",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of adult chitin-containing cuticle pigmentation",
                "id": "GO:0048082",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048082",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "calcium ion binding",
                "id": "GO:0005509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "hormone binding",
                "id": "GO:0042562",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042562",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JTM7",
                        "url": "https://www.uniprot.org/uniprotkb/A8JTM7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "A8JUP9-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A8JUP9",
                        "url": "https://www.uniprot.org/uniprotkb/A8JUP9"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 121,
        "chemical_mass": 13752.0,
        "gene_names": "CG6857;CG42302;CG6857;Dmel\\CG42302;Dmel_CG42302",
        "protein_name": "Mitochondrial import inner membrane translocase subunit",
        "disease": [
            {
                "disease_id": "DOID:0050757",
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                    {
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                ],
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                        "id": "E1JIY8",
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            },
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                    {
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                    {
                        "database": "UniProtKB",
                        "id": "Q6IKI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6IKI1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromosome segregation",
                "id": "GO:0007059",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007059",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6IKI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6IKI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "attachment of spindle microtubules to kinetochore",
                "id": "GO:0008608",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008608",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6IKI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6IKI1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "meiotic centromere clustering",
                "id": "GO:1990571",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990571",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6IKI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6IKI1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "E1JJL6-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "E1JJL6",
                        "url": "https://www.uniprot.org/uniprotkb/E1JJL6"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 100,
        "chemical_mass": 11683.0,
        "gene_names": "Dmel\\CG42512;CG42512;CG42528;Dmel\\CG42512;Dmel_CG42512;Dromel_CG32573_FBtr0074315_uORF",
        "protein_name": "Ashwin",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    },
    {
        "uniprot_canonical_ac": "M9NE97-1",
        "species": [
            {
                "name": "Drosophila melanogaster",
                "taxid": 7227,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "common_name": "Fruit fly",
                "glygen_name": "Fruit fly",
                "reference_species": "Drosophila melanogaster [7227]"
            }
        ],
        "length": 241,
        "chemical_mass": 26784.0,
        "gene_names": "Ctr1A;BcDNA:RH42635;CG3977;Ctr1A;DmCtr1A;Dmel\\CG3977;Dmel_CG3977;ctr1A",
        "protein_name": "Copper transport protein",
        "disease": [
            {
                "disease_id": "DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:0050700",
                "evidence": [
                    {
                        "id": "0050700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "copper ion transmembrane transport",
                "id": "GO:0035434",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035434",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular copper ion homeostasis",
                "id": "GO:0006878",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006878",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of heart rate",
                "id": "GO:0002027",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002027",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "copper ion transport",
                "id": "GO:0006825",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006825",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "copper ion import",
                "id": "GO:0015677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane copper ion transport",
                "id": "GO:0015679",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015679",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "copper ion transmembrane transporter activity",
                "id": "GO:0005375",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005375",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "M9NE97",
                        "url": "https://www.uniprot.org/uniprotkb/M9NE97"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "batch.fruitfly.9"
    }
]
